AU744292B2 - Cascade polymer complexes, process for producing the same and pharmaceuticals containing the same - Google Patents

Description

Our Ref.7520280 P/00/0IlI Regulation 3:2

AUSTRALIA

Patents Act 1990

ORIGINAL

COMPLETE SPECIFICATION STANDARD PATENT Applicant(s): Address for Service: Invention Title: Schering Aktiengesellschaft Patent Department D-13342 Berlin Germany DAVIES COLLISON CAVE Patent Trade Mark Attorneys Level 10, 10 Barrack Street SYDNEY NSW 2000 Cascade polymer complexes, process for producing the same and pharmaceuticals containing the same The following statement is a full description of this invention, including the best method of performing it known to me:- 5020 Cascade polymer complexes, process for producing the same and pharmaceuticals containing the same The invention relates to the object characterized in the claims, new cascade polymer complexes, agents that contain these compounds, the use of the complexes in diagnosis and therapy, and a process for the production of these compounds and agents.

The contrast media that are now used in clinical practice for the modern imaging processes of nuclear spin tomography (MRI) and computer tomography (CT) [Magnevist(', Pro Hance"*, Ultravist") and Omniscan"'] are dispersed in the entire extracellular space of the body (intravascular space and interstitium). This dispersion space comprises about 20% of the volume of the body.

In clinical practice, extracellular MRI contrast media were first used successfully in the diagnosis of cerebral and spinal disease processes since here a quite special situation exists i with respect to the regional dispersion space. In the brain and spinal cord, extracellular contrast media in healthy tissue do not leave the intravascular space because of the blood-brain barrier. In the case of pathological processes with disruption of the blood-brain barrier malignant tumors, inflammations, demyelinating diseases, etc.), regions with elevated blood-vessel permeability then develop inside the brain for these extracellular contrast media (Schmiedl et al., MRI of Blood-Brain Barrier Permeability in Astrocytic Gliomas: Application of Small and Large Molecular Weight Contrast Media, Magn. Reson. Med. 22: 288, 1991). Affected tissue can be identified with high contrast relative to healthy tissue by exploiting this disruption of vascular permeability.

Outside of the brain and the spinal cord, however, no such permeability barrier exists for the above-mentioned contrast media (Canty et al., First-Pass Entry of Nonionic Contrast Agent into the Myocardial Extravascular Space. Effects on Radiographic Estimate of Transit Time and Blood Volume. Circulation 84: 2071, 1991). Thus, the concentration of the contrast medium is no longer dependent on vascular pe rmeability, but only on the size of the extracellular space in the corresponding tissue.

Delimitation of the vessels relative to the surrounding interstitial space using this contrast medium is not possible.

A contrast medium that is dispersed exclusively in the vascular space would be desirable, particularly for the visualization of vessels. The purpose of such a blood-pool agent is to make it possible, with the aid of nuclear spin tomography, to delimit tissue with sufficient blood supply from tissue with insufficient blood supply, and-thus to diagnose an ischemia.

Infarcted tissue can also be delimited, based on its anemia, fromsurrounding healthy or ischemic tissue if a vasal contrast medium is used. This is of special importance if, the point is to distinguish a myocardial infarction from an ischemia.

To date, most of the patients in whom there is suspicion of cardiovascular disease (this disease is the most frequent cause .C of death in Western industrialized countries) have to undergo invasive diagnostic tests. In angiography at present, diagnostic radiology with the aid of iodine-containing contrast media is used in particular. These tests suffer from various drawbacks: they are associated with the risk of radiation exposure, as well as with difficulties and stresses, which therefore particularly have the effect that the iodine-containing contrast media, as compared with NMR contrast media, have to be used in much higher concentrations.

There is therefore a need for NMR contrast media which can mark the vascular space (blood-pool agents. These compounds are to be distinguished by good compatibility and by high effectiveness (high increase of signal intensity with MRI).

•Thus far, the attempt to solve at least a part of this problem by using complexing agents that are bonded to macromolecules or biomolecules has been successful only to a limited extent.

Thus, for example, the number of paramagnetic centers in the complexes that are described in European Patent Applications No.

0 088 695 and No. 0 150 844 is not sufficient for satisfactory imaging.

If the number of metal ions required is increased by repeated introduction of complexing units into a macromolecular biomolecule, this is associated with an intolerable impairment of the affinity and/or specificity of this biomolecule Nucl.

Med. 24, 1158 (1983)].

-~V&~4Th4~4V M~U~ Py~SW4ar~-.t-*A. Macromolecules can generally be suitable as contrast media j for angiography. Twenty-four hours after intravenous injection in rats, however, albumin-GdDTPA (Radiology 1987; 162: 205), shows a concentration in the liver tissue that constitutes almost 30% of the dose. In addition, only 20% of the dose is eliminated in 24 hours.

The macromolecule polylysine-GdDTPA (European Patent Application, Publication No. 0 233 619) has also proved suitable as a blood-pool agent. Because of production, however, this compound consists of a mixture of molecules of different sizes.

In excretion tests in rats, it was shown that this macromolecule is excreted unchanged by glomerular filtration through the kidneys. Due to factors related to synthesis, however, -j polylysine-GdDTPA may also contain macromolecules that are so large that they cannot pass through the capillaries of the kidneys in the case of glomerular filtration and thus remain in the body.

Also, macromolecular contrast media based on carbohydrates, dextran, have been described (European Patent Application, Publication No. 0 326 226). The drawback of these compounds lies in the fact that the latter generally carry only about 5% of the signal-enhancing paramagnetic cation.

The polymers described in European Patent Application No. 0 430 863 already represent a step toward blood-pool agents since they no longer exhibit the size and molecular weight relative to heterogeneity that are characteristic of the previously mentioned polymers. They leave something to be desired, however, as w-s regards complete elimination, compatibility, and/or S effectiveness.

The object was therefore to make available new diagnostic tools particularly to identify and locate vascular diseases that do not have the above-mentioned drawbacks. This object is achieved by this invention.

It has been found that complexes which consist of nitrogencontaining cascade polymers that are provided with complexing ligands, at least 16 ions of an element of atomic numbers 20-29, 39, 42, 44 or 57-83, and optionally cations of inorganic and/or organic bases, amino acids or amino acid amides, and which optionally contain acylated amino groups, are surprisingly very well suited for the production of NMR and x-ray diagnostic agents without exhibiting the above-mentioned drawbacks.

The complexing cascade polymers according to the invention can be described by general formula I W-K z,)y]x in which A stands for a nitrogen-containing cascade nucleus of base multiplicity a, X and Y, independently of one another, stand for a direct bond or a cascade reproduction unit of reproduction multiplicity x or y, Z and W, independently of one another, stand for a cascade reproduction unit of reproduction multiplicity z or w, K stands for the radical of a complexing agent, a stands for numbers 2 to 12, x, y, z and w, independently of one another, stand for numbers 1 to 4, provided that at least two reproduction units are different and that 16 a x y z w 5 64 holds true for the product of the multiplicities, and that at least one of cascadei reproduction units X, Y, Z and W stands for a 1,4,7,10-tetraazacyclododecane reproduction unit or 1,4,8,11-tetraazacyclotetradecane reproduction unit.

As cascade nucleus A, the following are suitable: nitrogen atom, U

U

2 2 2' p U S.

U

I 2 -CH2- -CH2CH N--CH U •U2 is n;~;r4;F

CH

2 -N

-H

2 -0H 2 -N 2(>2 N 1IC2H2 -N -H 2 -C .H 2 -N -H 2

CH-

2

-N

12 12 -N 2 -N -2H2 -N -0--H 2 0H 2 C 2 2 1 2 1 2 u

U

u u2

NN

12 12 U

U

N-M M-N 2 2Xur~ u Up

U

N-M 2- 21/ 2

UU

-U

R C(M-N

U

U NNN

U

2ZU 1-N.E r r r in which m and n stand for numbers 1 to p stands for numbers 0 to Ul stands for Ql or E,

U

2 stands for Q 2 or E with E meaning the group T(C2)o H 2

-N

whereby 0 stands for numbers 1 to 6, Q1 stands f or a hydrogen atom or Q 2 and

Q

2 stands for a direct bond, H stands for a CC 10 O alkylene chain which optionally is interrupted by 1 to 3 oxygen atoms and/or optionally is substituted with 1 to 2 oxo groups, R* stands f or a branched or unbranched C 1

-C

10 alkcyl radical, a nitro, amino, or carboxylic acid group or for

U

M-N

'2

U

whereby number Q 2 corresponds to base multiplicity a.

.:The nitrogen atom, whose three bonds (base multiplicity a= in a first "inner layer" (generation 1) are occupied by three reproduction units X or Y (if X stands for a direct bond) or Z (if X and Y in each case stand for a direct bond), represents the simplest case of a cascade nucleus; in other words: the threehydrogen atoms of the basic cascade starter ammonia A(H) g NH 3 have been substituted by three reproduction units X or Y or Z.

In this case, number Q 2 contained in cascade hucleus- A represents base multiplicity a.

Reproduction units X, Y, Z and W contain -NQ 1

Q

2 groups, in which Q 1 means a hydrogen atom or Q 2 and means a direct bond.

The number Q 2 contained in the respective reproduction unit X) corresponds to the reproduction multiplicity of this S .St~&w&S s, -At~ At-It Vt VtVV unit x in the case of The product of all multiplicities a *x y -z *w indicates the number of complexing agent radicals K bonded in the cascade polymers. The polymers according to the invention contain at least 16 and at most 64 radicals K in the molecule, which in each case can bond one ion to a maximum of three ions (in the case of divalent ions), preferably one ion, to an element of the above-mentioned atomic numbers.

The last generation, reproduction unit W bonded to complexing agent radical K, is bonded to K with NH groups (-NQ 1

Q

2 with Q 1 meaning a hydrogen atom and Q 2 direct bond),. while the preceding reproduction units can be linked together both by NHQ 2 groups by acylation reactions) and by NQ 2

Q

2 groups by alkylation reactions).

The cascade polymer complexes according to the invention exhibit a maximum of 10 generations more than just one of :reproduction units X, Y and Z can also be present in the molecule in each case), but preferably 2 to 4 generations, whereby at least two of the reproduction units in the molecule are different.

As preferred cascade nuclei A, those are indicated which fall under the above-mentioned general formulas if *M stands for numbers 1-3, especially preferably for number 1, 11 p stands.for numbers 0-3, especially preferably for numbers 1 and 3' o stands for numbers 1-2, especially preferably for number 1, M stands for a -CO or -CHCO group and Ro stands for a' -CHUIu 2

CH

3 or NO 2 group.

Preferred are al Cade nuclei A, which fall under the second and fourth of.the' indicated eight general formulas, especially those of general, :formula U72

N

!CO

U'

v' U2-Nj-OC CO-N 'U2 in which U' and U 2 stand for group E with o meaning number 1 or 2.

As further preferred cascade starters there can be listed, e.g.: (In the parentheses, base multiplicity a is indicated for the case where subsequent mono- or disubstitution is used in building the next generation) Tris(aminoethyl)amine (a 6 or 3); tris(aminopropyl)amine (a 6 or 3); diethylenetriamine (a 5.or 3); triethylenetetramine (a 6 or 4); tetraethylenepentamine (a 7 or a

S

S

a

S

9 a a.

a *a a a Y S VS g cvw, -v $V74S1r4 I- 1,3, 5-tris (aminomethyl) benzene (a 6 or 3); trimesic acid triamide (a 6 or 3); 1,4, 7-triazacyclorionane (a 3); 1O-tetraazacyclododecane (a 4); 1,4,7, 10, 13-pentaazacyclopentadecane (a 1,4,8, 11-tetraazacyclotetradecane (a 4); 1,4,7,1O,13,16-hexaazacyclooctadecane (a 6); 1,4,7,1O,13,16,19,22,25,28-decaazacyclotriacontane (a tetrakis (aminomethyl) methane (a 8 or 4); 1,1, 1-tris(aminomethyl) ethane (a =6 or 3); tris (aminopropyl) -nitromethane (a 6 or 3); 2,4, 6-triamino-1, 3, 5-triazine (a 6 or 3); 1,3,5, 7-adamantanetetracarboxylic acid amide (a 8 or 4); 3,3' -diphenylether-tetracarboxylic acid amide (a 8 or 4); 1, 2-bis(phenoxyetha ne)-3' acid amide (a 8 or 4); 1,4,7,10,13,16,21,24-octaazabicyclo[8.8.8]hexacosane (a It can be pointed out that the definition as cascade nucleus A and thus the separation of cascade nucleus and first reproduction unit can be selected by purely formal means and thus independently of the actual synthesis of the desired cascade polymer complexes. Thus, the tris(aminoethyl)amine used in Example 4 can be considered as cascade nucleus A itself (compare the general formula, indicated first for A, with m n p 1,

U

I E with o meaning number 1 and U1 U 2

Q

2 but also as a nitrogen atom cascade nucleus which as a first generation

/Q

exhibits three reproduction units H2 O-s N \Q2 oo*oo soS 0oo 5°5 *see Oev.

(compare the definition of E).

Cascade reproduction units X, Y, Z and W are determined, independently of one another, by

E,

3 U U-N 2

.U

1-U preferably -N E

OIE

-U

U

3

U-V

5U 1 U

U

-U

2

I

,preferably

/U

/UU

-CO-CH

U 2

U

6 t

N

N

UU N

U

6 t INUEi with t meaning number 1 or 2,

-CO(CH

2

U'

U-N

\2

U

-CO

U

U-N

2 preferably in which

U

1 stands for Q 1 or E,

U

2 stands for Q 2 or E with E meaning the group 1

-(CH

2 0

-CH

2

-N

Q.

whereby stands for numbers 1 to 6, preferably 1 to 2, stands for a hydrogen atom or Q2, :7"vn wwv-'.tf L ;J

Q

2 stands for a direct bond,

U

3 stands for an -NHCO-(CH 2 o chain or a C 1

-C

20 alkylene chain, preferably a CI-Clo alkylene chain, which optionally is interrupted by 1 to 10, preferably 1 to 2 oxygen atoms and/or 1 to 2 -N(CO)q-R 2 radicals, 1 to 2 phenylene radicals and/or 1 to 2 phenylenoxy radicals and/or optionally is substituted by 1 to 2 oxo, thioxo, carboxy, C 1 -Cg alkylcarboxy, alkoxy, hydroxy, C 1 alkyl groups, whereby q stands for numbers O or 1 and

R

2 stands for a hydrogen atom, a methyl or an ethyl radical, which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s), L stands for a hydrogen atom or the group

U

3

U-N

2 U 1 V stands for methine group -CH, if at the

I

same time U4 means a direct bond or group M and U 5 has one of the meanings of U 3 or

CO-

00- V stands for group -NH if at the °o*e* 'XIX iB same time U 4 and Us are, identical and mean the direct bond or group M, U51 sta nds for group M, and u6 stands for group

(CH)-N

or a direcdt,bn provided.:~:a es one of the cascade reproduction units stands. for, thie.I 147 1O-tetraazacyclododecane reproduction un'iiit .or" 1,4,8,1 1-tetraazacyclotetradecane reproduction unit that*-is indicated-above. In this case, 4,7, lO-tetraazacyclododecane reproduction unit is preferred., Pref erred cascade. reproduction units X, Y, Z and W are those in which in the above-mt itioned general formulas, radical U 3 stands for -COCH 2

OCH

2 CO-, -COCH 2 -CH CH 2

-CONHC

6

H

4 -NHCOCH,-, -COCH 2

CH

2 CO-, -COCH 2

-CH

2

CH

2 CO-, -COCH 2

CH

2

CH

2

CH

2

CO-,

-CONHCH

2

CH

2

NHCOCH

2 CH.CO-, -COCH 2

CH

2

NHCOCH

2

CH

2

CO-,

radical U4 stands for'a direct bond, for -CH 2

CO-,

radical US stands for a direct bond, for -(CH 2 4

-CH

2

CO-,

-CH (COOH) CH 2

OCH

2

CH

2

-CH

2

C

6

H

4

CH

2

-C

6

H

4

OCH

2 C2-, radical E stands for a group -C -OCH1 2

N

Cascade reproduction units X, Y, Z and W that are referred to as examples can be cited:

-CH

2

CH

2 NH-; -CH 2

CH

2

N<;

-COCH(NH-)(CH

2 4 NH-; -COCH(N< )(CH 2 4

N<;

-COCH

2

OCH

2

CON(CH

2

CH

2

NH-)

2

-COCH

2

OCH

2

CON(CH

2

CH

2 N< )2;

-COCH

2

N(CH

2

CH

2

NH.-

2

-COCH

2

N(CH

2

CH

2 N< )2;

-COCH

2 NH-; -COCH 2

N<C

-COC-H

2

CH

2

CON(CEI

2

CH

2

NH-)

2

-COCH

2

CH

2

CON(CH

2

CH

2 N< )2

-COCH

2

QCH

2

CONH-C

6

H

4

-CH[CH

2

CON(CH

2

CH

2 NH-)2] 2

-COC

2

OC

2

CONH-C

6 4

-CH[CH

2

CON(CH

2

CH

2 N< )2]2; -COCH2CH2CO-NH-C 6

H

4

-CH[CH

2

CON(CH

2

CH

2

NH-)

2 2 -COCH2CH 2

CO-NH-C.

6

H

4

-CH(CH

2

CON(CH

2

CH

2

N<)

2 2

-CONH-C

6

H

4

-CHCH

2

CON(CH

2

CH

2 NH-)2] 2

-CONH-C

6

H

4

-CH[CH

2

CON(CH

2

CH

2

N)

2 2 -COCH(NH-)CH(COOH)NH-; -COCH(N< )CH(COOH)N<; yyr~Zrt'r Wz.'t ~t -4~YA7VczA$.

18

CON(CH

2

GH

2

NH-)

2

-OOH

2 00H 2 00NH CON (CH 2

OH

2

NH-)

2

CONP(GH

2

GH

2 N< )2

-OOCH

2

OCH

2 00NH CON (CH 2

CH

2 2 -COCH 2

CH

2 CO N N- -COCHOCHC N-;

(~N

-COCH 2 CH CHCON N-

K~N

-COCH(CH CH CH -N)

-COCH(CH

2 CH.-N2 -Co

-COCH(CH

2 -N 2.

-N N

(N

-CQCH

2

CH

2 o- N -CO NHCOCH-N 2 NHCOCH 2

N_

r r r r r r r -CO N

N

I NO C NHCOCH

CH-N~

tra-%r~ yr W "I CON (GH 2

OH

2

NH-)

2 -CON -q N

H

2

ON

2

NH-)

2 CON (0H 2 01- 2 N <)2 -CONH q~ CON (CH 2 01-N<) 2

CON(OH

2

CH

2

NH-)

2 -COCH2

ON

2 WNH *N

H

-COoNOHCcH2NHNH

CON(W

2

C

2 N< )2

OCH

2

OH

2

NH-

-Co

OH

2

NH-

-co

OCH

2

CH

2

N<

OCH

2

CH

2

N<

OCH

2

CH

2

NH-

acH 2 a- 2

NHW,

O(CH

2 2 OH9NH

O(CH

2

CH

2

O)

2

CH

2 01H

OCH

2

CH

2

N<

O(O-

2

CH-

2 0) 2 H2CH 2

N<

/CO- (CH 2

CH

2 2

CH

2

CH

2

N<

O(O-I

2

O

2 2 CH2CH 2

N<

Complexing agent radicals K are described formiulas IA. IB and..IC:.

by general.

2 R OOC-R HC\NC 2 C N C* /2 CHR -00C OR'.

R

~CHR -00 OR (1A), R'OOC-HC HCO-a CH-COOR N -CH CH 2

-N-CHCH,-N

I

I

R'OOC-HC C--C OOR' (IB), (IB) R'OOC-H2C CH 2 -COOR CH 2

-CO

N -CH 2 CH -N -CHCH, -N R'OOC-H C CHaCOOR' (IC) in which R independently of one another, stand for a hydrogen atom or a metal ion equivalent of atomic numbers 20-29, 39, 42-44 or 57-83,

R

2 stands for a hydrogen atom, a methyl or an ethyl radical which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s),

R

3 stands for a R^ R 2 HCO 1N group, or a -CH -CO -N -U -T- R 4 -CH -CH -U -Tgroup,

OH

R

4 stands for a hydrogen atom or a straight-chain, branched, saturated or unsaturated C 1

-C

30 alkyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 phenylenoxy group and/or optionally is substituted by 1-5 hydroxy, 1-3 carboxy, 1-phenyl group(s 23

R

5 stands for a hydrogen atom or for R 4

U

7 stands for a straight-chain, branched, saturated or unsaturated CI-C 20 alkylene group optionally containing imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that optionally can be contained can be substituted by 1-2 carboxy, 1-2 sulfo or 1-2 hydroxy groups, T stands for a -CO-a, -NHCO-a or -NHCS-a group, and a stands for the binding site to the terminal nitrogen atoms of the last generation, of reproduction unit W.

Preferred are complexing agent radicals K of general formula

IA.

As preferred complexing agent radicals K, those can be mentioned in which in above-indicated formula IA, the C,-C 20 and preferably C,-C1, alkylene chain that stands for U 7 contains the groups

-CH

2

-CH

2 NHCO, -NHCOCH 2 O, -NHCOCH 2

OC

6 H4, -N(CH 2

CO

2

H),

-NHCOCH

2

C

6

H

4

-NHCSNHC

6

H

4 -CHC -CH 2 CH20 and/or is substituted by groups -COOH, -CH 2

COOH.

*o i -x -rns, .S~tf--T As examples of U 7 the following groups can be cited:

-CH

2

-CH

2

CH

2

-CH

2

CH

2

CH

2

-C

6

H

4 -9 -C 6

H

1 0

-CH

2

C

6

H

5

-CH

2

NHCOCH

2

CH(CH

2

CO

2

H).C

6

H

4

-CH

2

NHCOCH

2

OCH

2

-CH

2

NHCOCH

2

C

6

H

4

-CH

2

NHCOCH

2 C0 2

H

-CH2NHCSNH-C 6

H

4

-CH(CH

2

COOH)CH

2

-CH

2

OC

6

H

4

-N(CH

2

COOH)CH

2

-CH

2

NHCOCH

2 O(CH2CH 2

O)

4

.C

6

H

4

-C

2

O-C

6

H

4

-CH

2

CH

2

-O-CH

2

CH

2

-CH

2 CH2-O-CH-)CI 4-O--CH,CH C0 2

H

S0 3

H

a.

a a a a a

U

7 is especially preferred for the CH. group.

As examples of R 4 the following groups can be indicated:

-CH

3

-C

6

H

5

-CH

2

-COOH,

-CH

2

-C

6

H

5

-CH

2

-O-(CH

2

CH

2 6

CH

3

-CH

2

-OH

Pref erred are the hydrogen atom and the methyl'group, and T preferably stands for the -CO-a group.

-J

If the agent according to the invention is intended for use in NMR diagnosis, the central ion of the complex salt must be paramagnetic. These are especially the divalent and trivalent ions of the elements of atomic numbers 21-29, 42, 44, and 58-70.

Suitable ions are, for example, the chromium(III), iron(II), cobalt(II), nickel(II), copper(II), praseodymium(III), neodymium(III), samarium(III), and ytterbium(III) ions. Because of their very strong magnetic moment, the gadolinium(III), terbium(III), dysprosium(III), holmium(III), erbium(III), manganese(II), and iron(III) ions are especially preferred.

If the agent according to the invention is intended for use in diagnostic radiology, the central ion has to be derived from an element of higher atomic number in order to achieve sufficient absorption of the x rays. It has been found that for this purpose, diagnostic agents which contain a physiologically compatible complex salt with central ions of elements of atomic numbers between 21-29, 39, 42, 44, 57-83 are suitable; these are, for example, the lanthanum(III) ion and the above-mentioned ions of the ianthanide series.

oo*: I. The cascade polymer complexes according to the invention contain at least 16 ions of an element of the above-mentioned atomic numbers.

The remaining acid hydrogen atoms, those which were not substituted by the central ion, optionally can be replaced completely or partially by cations of inorganic and/or organic bases, amino acids, or amino acid amides.

Suitable inorganic cations are, for example, the lithium ion, the potassium ion, the calcium ion, the magnesium ion, and especially the sodium ion. Suitable cations of organic bases are, those of primary, secondary, or tertiary amines, such as, for example, ethanolamine, diethanolamine, morpholine, glucamine, N,N-dimethylglucamine, and especially Nmethylglucamine. Suitable cations of amino acids are, for example, those of lysine, arginine, and ornithine, as well as the amides of otherwise acidic',or neutral amino acids.

The compounds according'to the invention, which have a molecular weight.of..10,00. 80000 D, preferably 15,000-40,000 D, exhibit the desired properties described above. They contain the large number, required for their use, of metal ions bonded in a stable manner to the complex..l They accumulate in regions with high vascular permeability, such as, in tumors, they make it possible to make statements regarding the perfusion of tissues, and they provide the possibility of determining the blood volume in tissues, of shortening selectively the relaxation times or densities of the blood, and of graphically representing the permeability of blood vessels. Such physiological data cannot be obtained through the use of extracellular contrast media, such as, Gd-DTPA [MagnevistR)1. From these standpoints, there also follow the uses in the modern imaging processes of nuclear spin tomography and computer tomography: more specific diagnoses of malignant tumors, early therapy monitoring in cases where cytostatic, t antiphlogistic, or vasodiiative therapy is used, early identification of underperfused regions in the myocardium), angiography in vascular diseases, and identification and diagnosis of (sterile or infectious) inflammations.

As further advantages relative to extracellular contrast media, such as, Gd-DTPA [Magnevist(R)], the greater effectiveness as contrast media for nuclear spin tomography (higher relaxivity) must be emphasized; this ensures a marked reduction of the diagnostically required dose. At the same time, the contrast media according to the invention can be formulated as solutions in an isoosmolar manner in the blood and thus reduce the osmotic stress of the body, which is reflected in a reduced toxicity on the part of the substance (higher toxic threshold).

Smaller doses and higher toxic thresholds result in a significant increase of the reliability of contrast medium use in modern imaging processes.

In comparison with macromolecular contrast media based on carbohydrates, dextran (European Patent Application, Publication No. 0 326 226), which carry as mentioned generally only about 5% of the signal-enhancing paramagnetic cation, the polymer complexes according to the invention exhibit a content of the paramagnetic cation of generally about Thus, the macromolecules according to the invention produce much better signal enhancement per molecule, which simultaneously has the effect that the dose necessary for nuclear spin tomography is considerably smaller relative to macromolecular contrast media based on carbohydrates.

0° O• SgT:7~VZ 28 With the polymer complexes according to the invention, it has been possible to design and produce macromolecules in such a way that the latter have a uniformly defined molecular weight.

It is thus possible, surprisingly enough, to control the size of the macromolecules in such a way that the latter are large enough to be able to leave the vascular space only slowly, but at the same time small enough to be able to pass through the capillaries of the kidneys, which are 300-800 A in size.

In comparison to the other mentioned polymer compounds of the prior art, the cascade polymer complexes according to the invention are distinguished by improved excretion behavior, greater effectiveness, greater stability, and/or better compatibility.

Another advantage of this invention lies in the fact that now complexes with hydrophilic or lipophilic, macrocyclic or open-chain, low-molecular, or high-molecular ligands have become accessible. As a result, the possibility exists for controlling the compatibility and pharmacokinetics of these polymer complexes by chemical substitution.

0 The production of the cascade polymer complexes according to the invention is carried out in that compounds of general formula

I'

W-B) which A stands for a nitrogen-containing cascade nucleus of base multiplicity a, e X and Y, independently of one another, stand for a direct bond or a cascade reproduction unit of reproduction multiplicity x or y, Z and W, independently of one another, stand for a cascade reproduction unit of reproduction multiplicity z or w, a stands for numbers 2 to 12, x, y, z and w, independently of one another, stand for numbers 1 to 4 and B stands for the binding site of the terminal NH groups of the last generation, of reproduction unit W provided that at least two reproduction units are different, and that for the product of multiplicities, 16 a x y z w 5 64, holds true, and that at least one of cascade reproduction units X, Y, Z and W stands for a 1,4,7,10-tetraazacyclododecane reproduction unit or a 1,4,8,11-tetraazacyclotetradecane reproduction unit, are reacted with a complex or complexing agent K' of general formula I'A, I'B or I'C R l 2/ 3- 2 .2

C-H

2 2.

I I (IA) N-C--C H- O O Ol-C OR i s a

CHCO.

R'OOC-H

ROOC-H2 2 C C I I I N -CH CH 2

N-CH

2

CH

2

N

I

H,-COOR'

H

2 -C OOR 1

C

I C! R'OOC-H C

CH,-COOR

CH-C*O-

N -CH2CH -N CH 2

CH

2

N

II

(I'C)

COOR

1 R'OOC-H2C Ct whereby

R

1 independently of one another, stand for a hydrogen atom, a metal ion equivalent of atomic numbers 20-29, 39, 42-44, or 57-83 or an acid protective group,

R

2 stands for a hydrogen atom, a methyl or an ethyl radical which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s),

R

3 stands for a

R

4

R

2 I g -CH -CO-N -U group or a r r -CH -CH group

O

OH

r

R

4 stands for a hydrogen atom or a straight-chain, branched, saturated or unsaturated C 1

-C

3 alkyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 phenylenoxy group and/or optionally is substitutedby 1-5 hydroxy, 1-3 carboxy, 1-phenyl group(s),

R

5 stands fora, hydrogen atom or for R 4

U

7 stands for a straight-chain, branched, saturated or unsaturated C-C alkylene group optionally containing imino,, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenyleniino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that are optionally contained can be substituted by 1-2 carboxy, 1-2 sulfo or 1-2 hydroxy groups, T' stands for a -COOH, -N=C=O or -N=C=S group, and C*O stands for an activated carboxyl group, provided that-- if K' stands for a complex at least two (in the case of divalent metals) or three (in the case of trivalent metals) of substituents R 1 stand for a metal ion equivalent of'the above-mentioned elements and that optionally other. carboxyl. groups are present in the form of 455 ;-rjypw their salts with inorganic and/or organic bases, amino acids or amino acid amides, optionally present protective groups are cleaved of f, the thus obtained cascade polymers if K' stands for a complexing agent -are reacted in a way known in the art with at least one metal oxide or metal salt of an element of atomic numbers 20-29, 39, 42, 44, or 57-83 and then optionally in the cascade polymer complexes thus obtained, acid hydrogen atoms that are still present are completely or partially substituted by cations of inorganic and/or organic bases, amino acids, or amino acid amnides, and optionally still present free terminal amino groups are optionally acylated before or after the metal complexing.

Another aspect of this invention is represented by the new compounds of general formula I'A 3.

R

R OOC-R HC N -CH 2 -CH2 -N 1 1 CH,

CH,

2 (I'A 1N-CH 2

-H

2

-N

/2 2R CHR -CO OR CHR -COOR whereby independently of one another, stand for a hydrogen atom, a metal ion equivalent of atomic numbers 20-29, 39, 42-44 or 57-83 or an acid protective group,

R

2 stands for a hydrogen atom, a methyl or an ethyl radical, which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s),

R

3 stands for a

R

4

R

2 I

I

-CH CO -N -U group or a

R

4 -CH -CH group,

O

OH

R

4 stands for a hydrogen atom or a straight-chain, branched, saturated or unsaturated C,-C 0 alkyl chain, which optionally is interrupted by 1-10 oxygen atoms, 1 phenylene group, 1 phenylenoxy group and/or optionally is substituted by 1-5 hydroxy, 1-3 carboxy, 1-phenyl group(s), U stands for a straight-chain, branched, saturated or unsaturated alkylene group optionally containing imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, sulfur and/or 1-5 nitrogen atom(s) and/or optionally substituted by 1-5 hydroxy, 1-2 mercapto, 1-5 oxo, thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s), whereby the phenylene groups that are optionally contained can be substituted by 1-2 carboxy, 1-2 sulfo or 1-2 hydroxy groups, T' stands for a -COOH, -N=C=O or -N=C=S group, and C*O stands for an activated carboxyl group.

They are used as important intermediate products for the production of the cascade polymer complexes of general formula I.

As an example of an activated carbonyl group C*O in complexes or complexing.agents anhydride, p-nitrophenyl ester, N-hydroxysuccinimide ester, pentafluorophenyl ester, and acid chloride can be mentioned.

c'r -e nr *tr V5%- y vt The addition or acylation that is carried out to introduce the complexing agent units is performed with substrates that contain desired substituents K (optionally bonded to a leaving group) or from which the desired substituent is generated by the reaction.

As examples of addition reactions, the reaction of isocyanates and isothiocyanates can be mentioned, whereby the reaction of isocyanates is preferably performed in aprotic solvents, such as, THF, dioxane, DMF, DMSO, methylene chloride at temperatures of between 0 and 100 0 C, preferably between 0 and 50 0 C, optionally with the addition of an organic base such as triethylamine, pyridine, lutidine, Nethyldiisopropylamine, N-methylmorpholine. The reaction with isothiocyanates is generally performed in solvents, such as, water or lower alcohols, such as, methanol, ethanol, isopropanol or their mixtures, DMF or mixtures of DMF and water at temperatures of between 0 and 100°C, preferably between 0 and 0 C, optionally with the addition of an organic or inorganic base, such as, triethylamine, pyridine, lutidine, Nethyldiisopropylamine, N-methylmorpholine, or alkaline-earth hydroxides, alkali hydroxides, such as, lithium, sodium, potassium, calcium hydroxide, or their carbonates, such as, e.g., magnesium carbonate.

As examples of acylation reactions, the reaction of free carboxylic acids according to the methods known to one skilled in the art J. P. Greenstein, M. Winitz, Chemistry of the Amino Acids, John Wiley Sons, N.Y. (1961), pp. 943-945] can be 7 ~rr~~ mentioned. It has proven advantageous, however, to convert the carboxylic acid group before the acylation reaction into an activated form, such as, anhydride, active ester or acid chloride E. Gross, J. Meienhofer, The Peptides, Academic Press, N.Y. (1979), Vol. 1, pp. 65-314; N. F. Albertson, Org.

React. 12, 157 (1962)].

In the case of rection with active ester, the literature known to one skilled in'the art Houben-Weyl, Methoden der organischen Chemie [Methods of Organic Chemistry], Georg Thieme Verlag, Stuttgart, Volume t15' (1985), 633] can be cited. This reaction can be performed unider the conditions indicated above for the anhydride reaction.. Aprotic solvents, such as, e.g., methylene chloride, .chloroform, however, can also be used.

In the case of acidchloride reactions, only aprotic solvents, such as, methylene chloride, chloroform, toluene or THF, at temperatures. of between -20 to 50 0 C, preferably of between 0 to 30 0 C, are used. Further, literature known to one skilled in the art Houben-Weyl, Methoden der Organischen Chemie, Georg-Thieme-Verlag, Stuttgart, (1974), Volume 15/2, pp.

355-364] can be cited.

If R 1 stands for an acid protective group, lower alkyl, aryl and aralkyl groups, for example, the methyl, ethyl, propyl, butyl, phenyl, benzyl, diphenylmethyl, triphenylmethyl, bis-(pnitrophenyl)-methyl groups, as well as trialkylsilyl groups, are suitable.

The optionally desired' cleavage of the protective groups is .coi carried out according to. ,the processes known to one skilled in the art, for example by hydrolysis, hydrogenolysis, alkaline saponification of esters with alkali in aqueous-alcoholic solution at temperatures of 0 0 C to 50 0 C or in the case of tertbutyl esters with the aid of trifluoroacetic acid.

Terminal amino groups that are optionally incompletely acylated with ligands or complexes can optionally be converted into amides or semiamides. The reactions with acetic anhydride, succinic acid anhydride or diglycolic acid anhydride can be mentioned as examples.

The introduction of the desired metal ions is carried out in the way in which it was disclosed in, German Laid-Open Specification 34 01 052, by the metal oxide or a metal salt (for example, the nitrate, acetate, carbonate, chloride or sulfate) of the element of atomic numbers 20-29, 42, 44, 57-83 being dissolved or suspended in water and/or a lower alcohol (such as methanol, ethanol or isopropanol) and being reacted with the solution or suspension of the equivalent amount of complexing ligand and then, if desired, existing acid hydrogen atoms of the acid groups being substituted by cations of inorganic and/or organic bases, amino acids or amino acid amides.

The introduction of the desired metal ions can be carried out both in the stage of complexing agent I'A or I'B, i.e., .0.

before the coupling to the cascade polymers, and after coupling 9oo.

of unmetalated ligands I'A, I'B or I'C.

S.00. In this case, the neutralization is carried out with the aid of inorganic bases (for example, hydroxides, carbonates or Goes"r xi e ar o at s o bicarbonates) of, for example, sodium, potassium, lithium, sees magnesium or calcium and/or organic bases, such as, i.a., primary, secondary and tertiary amines, such as, for example, ethanolamine, morpholine, glucamine, N-methyl and N,Ndimethylglucamine, as well as basic amino acids, such as, for example, lysine, arginine and ornithine or of amides of originally neutral or acidic amino acids, such as, for example, hippuric acid, glycine acetamide.

For the production of neutral complex compounds, enough of the desired bases can be added, for example, to the acid complex salts in aqueous solution or suspension that the neutral point is reached. The obtained solution can then be evaporated to the dry state in a vacuum. Often, it is advantageous to precipitate the neutral salts formed by adding water-miscible solvents, such as, for example, lower alcohols (methanol, ethanol, isopropanol, etc.), lower ketones (acetone, etc.), polar ethers o (tetrahydrofuran, dioxane, 1,2-dimethoxyethane, etc.) and thus to obtain easily isolated and readily purified crystallizates. It has proven especially advantageous to add the desired bases as early as during the complexing of the reaction mixture and thus to save a process step.

If the acid complex compounds contain several free acid groups, it is often suitable to produce neutral mixed salts, which contain both inorganic and organic cations as counterions.

This can happen, for example, by the complexing ligands in aqueous suspension or solution being reacted with the oxide or salt of the element yielding the central ion and half of the a o amount of an organic base required for neutralization, the go complex salt formed being isolated, optionally purified and then mixed with the required amount of inorganic base for complete neutralization. The sequence of the addition of base can also be reversed.

The purification of the thus obtained cascade polymer .ompnlexes is carried out, optionally after adjusting the pH to 6 to preferably about 7, by adding an acid or base, preferably .by ultrafiltration with membranes of suitable pore size Amicon("YM10, AmiconCR)YM3) or gel filtration on, suitable Sephadex") gels.

In the case of neutral complex compounds, it is often advantageous to provide the polymeric complexes with an anion :exchanger, for example, IRA 67 (OH" form) and optionally in Saddition with a cation exchanger, for example, IRC 50 form) for the separation of ionic components.

The production of the cascade polymers carrying terminal amino groups required for the coupling to complexing agents K' (or else the corresponding metal-containing complexes) generally proceeds from nitrogen-containing cascade starters that can be produced by commercially available methods or according to or analogously to methods known in the literature. The introduction "*oe of generations X, Y, Z and W is carried out according to methods known in the literature J. March, Advanced Organic.

Chemistry, 3rd Ed.; John Wiley Sons, (1985), 364-381] by acylation or alkylation reactions with protected amines exhibiting the desired structures, which contain functional groups capable of bonding to the cascade nuclei, such as, e.g.,

-U

-i *3 'J carboxylic acids, isocyanates, isothiocyanates or activated carboxylic acids (such as, anhydrides, active esters, acid chlorides) or halides (such as, chlorides, bromides, iodides), aziridine, mesylates, tosylates or other leaving groups known to one skilled in the art.

It can be stressed, however, that the differentiation between cascade nucleus A and reproduction units is purely formal. It can be advantageous synthetically that formal cascade starter A(H)a is not used, but rather the nitrogen atoms forming part of the cascade nucleus by definition are introduced first together with the first generation. Thus, for synthesis of the compound described in Example Ib), it is more advantageous not to alkylate the formal cascade nucleus trimesic acid triamide with, benzyloxycarbonylaziridine (six-fold), but rather to react trimesic acid trichloride with bis(2- (benzyloxycarbonylamino)-ethyl]-amine (three-fold).

In the same way, with the incorporation of the necessarily present 1,4,7,10-tetraazacyclododecane ("cyclene") or 1,4,8,11tetraazacyclotetradecane ("cyclam") reproduction units, it can be advantageous not to synthesize the cascade polymer formally shell for shell.

Thus, it is possible, for example, in an upstream reaction step, to bind the reproduction unit following a cyclene shell to three nitrogen atoms of the cyclene. Then, after functionalization of the fourth cyclene-nitrogen, both reproduction units can be linked simultaneously to the increasing cascade.

41 As amine protective groups, the benzyloxycarbonyl, tertbutoxycarbonyl, trifluoroacetyl, fluorenylmethoxycarbonyl, benzyl and formyl groups familiar to one skilled in the art [Th. W.

Greene, P. G. M. Wuts, Protective Groups in Organic Syntheses, 2nd Ed., John Wiley and Sons (1991), pp. 309-385] can be mentioned. After cleavage of these protective groups, which also is carried out according'o methods known in the literature, the next desired generation can be introduced into the molecule. In addition to this synthesis of a generation consisting of two reaction stages in, each 'case (alkylation or acylation and S protective group cleavage the simultaneous introduction of two, X-[Y]x or several generations, X-[Y-(Z)y]x is also possible with only two reaction stages. The synthesis of these multi-generation units is carried out by alkylation or acylation of unprotected amines ("reproduction amine"), exhibiting the structures of the desired reproduction units, with a second reproduction amine, whose amine groups are present in protected form.

The compounds of general formula required as cascade starters are commercially available or can be produced according S to or analogously to methods known in the literature Houben-Weyl, Methoden der Org. Chemie, Georg-Thieme-Verlag, o.

Stuttgart (1957), Vol. 11/1; M. Micheloni et al., Inorg. Chem.

(1985), 24, 3702; T. J. Atkins et al., Org. Synth., Vol. 58 (1978), 86-98; The Chemistry of Heterocyclic Compounds: J. S.

Bradshaw et al., Aza-Crown-Macrocycles, John Wiley Sons, N.Y.

*o I A 4' .,YA 4*A V- 42 (1993)]. As examples, there can be cited: Tris(aminoethyl)amine Fluka Chemie (Fluka Chemistry] AG, Switzerland; Aldrich-Chemie (Aldrich Chemistry], Germany]; tris(aminopropyl)amine C. Woerner et al., Angew.

Chem. (Applied Chem.] Int. Ed. Engle (1993)-, 12, 1306]; diethylenetriamine Fluka; Aldrich]; triethylenetetramine Fluka; Aldrich]; tetraethylenepentauine Fluka; Aldrich]; 1,3,5-tris(aminomethyl)benzene T. M. Garrett et al., J. Am. Chem. Soc. (1991), 113, 2965]; trimesic acid triamide H. Kurihara; Jpn. Kokai Tokyo Koho JP 04077481; CA 11,162453]; 1,4,7-triazacyclononane Fluka; Aldrich]; 1,4,7,10, 13-pentaazacyclopentadecane K. We Aston, Eur. Pat. Apple 0 524 161, CA 120, 44580]; 1,4,7, 10-tetraazacyclododecane Aldrich] 1,4,8, 11-tetraazacyclotetradecane Fluka; Aldrich]; l, 4 ,7,lO,l 3 ,l 6 ,l 9 2 2,25,28-decaazacyclotriacontane A. Andres et al., J. Chem. Soc. Dalton Trans. (1993), 3507]; As.1,1,1-tris(aminomethyl)ethane Re J. Geue et al., As.J. Chem. (1983), 36, 927]; tris (aminopropyl) -nitromethane G. R. Newkome et al., Angew. Chem. 103, 1205 (1991) analogously to Re C. Larock, Comprehensive Organic Transformations, VCH Publishers, N.Y.

(1989), 419-420] ~~c~Ai7r.%tsz-r~ z l,3,5,7-adamantaretetracarboxylic acid amide

H.

Stetter et al., Tetr. Lett. 1967, 1841]; 1,2-bisphenoxyethane-3I,3I 1,5' ,51-tetracarboxylic acid amide 3. P. Coliman et al.; J. Am. Chem. Soc. (1988), 110, 3477-86 analogously to the instructions for Example Ib)]; 1,4,7,10,1 3 ,l 6 ,2l,24-octaazabicyclo[8.8.8]hexacosane P. H. Smith et al., J. Org. Chem. (1993), 58, 7939].

The production of the reproduction amines that contain the above-mentioned functional groups required for the synthesis of generations is carried out according to or analogously to the i: instructions described in the experimental part or according to processes known in the literature.

As examples, there can be mentioned: Na,N -Di-benzyloxycarbonyl-lysine-p-ni ester;

HOOC-CH

2

OCH

2 CO-N (CH 2

CH

2

NH-CO-O-CH

2

C

6

H

5 2

HOOC-CH

2 N (CH 2

CH

2

NH-CO-O-CH

2

C

6 2

HOOC-CH

2

CH

2 CO-N (CH 2

CH

2

NH-COCF

3 2 [to be produced according to instructions for Example 5a), by starting from bis(trifluoroacetylaminoethyl)amine instead of bis(benzyloxycarbonylaminoethyl)amine];

HOOC-CH

2 0CH 2

CONH-C

6

H

4 -CH [CH 2 CON (CH 2

CH

2

NH-CO--CH

2

C

6 2

O=C=N-C

6

H

4 -CH CH 2 CON (CH 2

CH

2 NH-CO-o-CH 2

C

6

H

5 2 1 2 0 NH-CO-0-CH

C

6

H

C

01C NH-CO-0-CH 2 C

H

C.

h C CON (CH 2

CH

2

NH-CO-O-CH

2

CH,)

2

HOOC-CH

2 00H 2 CONH CON (CH CH 2

NH-CO-O.CH

2

CH

5 CON (CH 2

CH

2

NH-CO-O-CH

2 05H 5 2 CON (CH 2

OH

2 NH.-OcH 2

CH

5 2 N-benzyloxycarbonyl-aziridine to be produced according to.M.

Zinic et al., J. Chem. Soc, Perkin Trans 1, 21-26 (1993) N-benzyloxycarbonyl-glycine commercially available in, e-g., Bachem, California

OCH

2

CH

2 NHOO-O-0H 2

C

6

H

HOOC OCHCH 2 NHOO-O-0H 2

C

6

H

5

OGH

2

CH

2

NHCO-O-CH

2

C

6

H

5

S

to be produced according to C. J.

Cavallito, et al., J. Amer. Chem. Soc.

1943, 2140, by starting from N-CO-O-

CH

2

C

6

H

5 (2-bromoethyl) amine, instead of benzyl chloride R. Jacobson et al., J. Med. Chem. (1991), .34, 2816].

The production of the complexes and complexing agents of general formula I'A and I'B is carried out according to or analogously to the instructions described in the experimental part or according to methods known in the literature (see, e.g., European Patent Applications Nos. 0 512 661, 0 430 863, 0 255 471 and 0 565 930.

Thus, the production of compounds of general formula I'A can be carried out, in that a group T" is used as a precursor of functional group either in the meaning of a protected acid function, which can be converted into the free acid function S independently of acid protective groups R 1 according to the above-indicated process, or in the meaning of a protected amine function, which unblocks according to processes known in the literature [Th. W. Greene, P. G. M. Wuts, Protective Groups in Organic Synthesis, 2nd Edition, John Wiley Sons (1991), pp.

309-385] and then can be converted into the isocyanates or isothiocyanates [Methoden der Org. Chemie (Houben-Weyl), E 4, pp.

742-749, 837-843, Georg Thieme Verlag, Stuttgart, New York (1983)]. Such compounds can be produced according to or analogously to the instructions that are described in the experimental part by monoalkylation of cyclene with suitable a- Shaloacid amides [in aprotic solvents, such as, chloroform].

The production of compounds of general formula I'B can be carried out, for example, in that a protected acid function is I- used as a precursor of the activated carboxyl group-C*O, which can be converted into the free acid function independently of acid protective groups R' according to the above-indicated processes and can be activated according to the processes that are known in the literature and are also described above. Such compounds can be produced according to or analogously to the instructions that are 'decribd in the experimental part or, for example, in that an amiio acid derivative of general formula II

R

(II)

o. 1. H,N CO2V in which

R

5 has the meaning indicated for R 5 whereby hydroxy or carboxy groups that :are optionally contained in R 5 are optionally present in protected form, and

V

1 is a straight-chain or branched C1-C6 alkyl group, a benzyl, trimethylsilyl, triisopropylsilyl, 2,2,2trifluoroethoxy or 2,2,2-trichloroethoxy group, whereby

V

I is different from is reacted with an alkylating agent of general formula III

CO

2

R

1

(COIR

Hal N in which

R

1 stands for a protective group, and k C'T. $iCafa- 47 Hal stands for a halogen atom, such as Cl, Br or I, but preferably Cl [see also M. A. Williams, H.

Rapoport, J. Org. Chem. 58, 1151 (1993)].

Preferred amino acid derivatives are the esters of naturally occurring a-amino acids.

The reaction of compound (II) with compound (III) is carried out preferably in a buffered alkylation reaction, whereby an aqueous phosphate-buffer solution is used as a buffer. The reaction is carried out at a pH of 7-9, but preferably at a pH of 8. The buffer concentration can be between 0.1-2.5 M, but 'preferably a 2 N phosphate-buffer solution is used. The temperature of the alkylation can be between 0 and 50 0 C; the S preferred temperature is room temperature.

The reaction is carried out in a polar solvent, such as, acetonitrile, tetrahydrofuran, 1,4-dioxane or 1,2- S dimethoxyethane. Preferably, acetonitrile is used.

The production of the pharmaceutical agents according to the invention is also carried out in a way known in the art, by the complex compounds according to the invention optionally with the addition of the additives that are commonly used in galenicals being suspended or dissolved in aqueous medium and then the suspension or solution optionally being sterilized.

Suitable additives are, for example, physiologically harmless buffers (such as, for example, tromethamine), additives of complexing agents or weak complexes (such as, for example, diethylenetriaminepentaacetic acid or the corresponding Cacascade polymer complexes) or if necessary electrolytes, 7 such as, for example, sodium chloride or if necessary antioxidants, such as, for example, ascorbic acid.

If suspensions or solutions of the agents according to the invention in water or physiological salt solution are desired for enteral administration or other purposes, they are mixed with one or more adjuvant(s) that are commonly used in galenicals [for example, methyl cellulose, lactose, mannitol] and/or surfactant(s) (for example, lecithins, Tween(R Myrj(R)] and/or flavoring substance(s) for taste correction [for example, ethereal oils].

:In principle, it is also possible to produce the pharmaceutical agents according to the invention even without isolating the complex salts. In any case, special care must be used to undertake the chelation so that the salts and salt solutions according to the invention are practically free of noncomplexed metal ions having a-toxic effect.

This can be ensured, for example, with the aid of color indicators such as xylenol orange by control titrations during the production process. The invention therefore also relates to processes for the production of complex compounds and their salts. As a last precaution, there is a purification of the :0 isolated complex salt.

The pharmaceutical agents according to the invention contain preferably 1 gmol-1 mol/l of the complex salt and are generally see 0 dosed in amounts of 0.0001-5 mmol/kg. They are intended for .CC. enteral and parenteral administration. The complex compounds -v 49 according to the invention are used 1. for NMR diagnosis and diagnostic radiology in the form of their complexes with the ions of elements with atomic numbers 21-29, 39, 42, 44 and 57-83; 2. for radiodiagnosis and radiotherapy in the form of their complexes with radioisotopes of the elements with atomic numbers 27, 29, 31, 32, 37-39, 43, 49, 62, 64, 75 and 77.

The agents according to the invention meet the varied requirements for suitability as contrast media for nuclear spin tomography. Thus, they are very well suited, after oral or parenteral administration, for improving the image, obtained with the aid of nuclear spin tomographs, in its informative value by increasing the signal intensity. Further, they show the great ***effectiveness which is necessary to load the body with the fewest too to possible amounts of foreign substances, and the good compatibility which is necessary to maintain the noninvasive nature of the studies.

The good water solubility and low osmolality of the agents according to the invention makes it possible to produce highly concentrated solutions, so that the volume load of the circulatory system can be held within reasonable limits, and to compare the dilution through the bodily fluid,

NM

diagnostic agents must be 100- to 1000-fold better water-soluble than for NMR spectroscopy. Further, the agents according to the invention exhibit not only high stability in vitro, but also too. surprisingly high stability in vivo, so that a release or an ThV$~Vkt exchange of the ions toxic in themselves not covalently bonded in the complexes is carried out only extremely slowly within the time in which the new contrast media are again completely excreted.

In general, the agents according to the invention for use as NMR diagnostic agents are dosed in amounts of 0.0001 5 mmol/kg, preferably 0.005-0.5 mmol/kg. Details of use are discussed in, for example, Weinmann et al., Am. J. of Roentgenology 142, 619 (1984).

t" Especially. low dosages (under 1 mg/kg of body weight) of organ-specific NMR diagnostic agents can be used, for example, to detect tumors and myocardial infarction.

Further, the complex compounds according to the invention are used advantageously as susceptibility reagents and as shift reagents for in vivo NMR spectroscopy.

The agents according to the invention are also suitable as radiodiagnostic agents because of their advantageous radioactive o. properties and the good stability of the complex compounds contained in them. Details of their use and dosage are described in, "Radiotracers for Medical Applications," CRC Press, Boca Raton, Florida.

090.90 *00 Another imaging method with radioisotopes is positron 9o99 emission tomography, which uses positron-emitting isotopes, such as, 43 Sc, "Sc, 5 "Fe, 55 Co and 6Ga (Heiss, W. Phelps, M.

Positron Emission Tomography of Brain, Springer Verlag Berlin, Heidelberg, New York 1983).

00* a.

b 0 0 0* 9 The compounds according to the invention are,also suitable, surprisingly enough, for differentiating malignant and benign tumors in areas without blood-brain barriers.

They are also distinguished in that they are eliminated completely from the body and thus are well-tolerated.

Since the substances according to the invention are concentrated in malignanf'tioturs (no diffusion in healthy tissue, but high permeability of tumor vessels), they can also assist in the radiation therapy of malignant tumors. The latter is S distinguished from the corresponding diagnosis only by the amount and type of the isotope usd. The object, in this case, is the destruction of tumor cells by high-energy shortwave radiation with a smallest possible range of action. For this purpose, interactions of theimetals.contained in the complexes (such as, iron or gadolinium) are used with ionizing radiations x rays) or with.neutron rays. By this effect, the local radiation dose is significantly increased on the spot where the metal complex is found in tumors). To produce the same radiation dose in the malignant tissue, the radiation exposure for healthy tissue can be considerably reduced with the use of such metal complexes and thus side effects that are stressful to the patients are avoided. The metal complex conjugates according to the invention are therefore suitable also as radiosensitizing substances in radiation therapy of malignant tumors use of MSssbauer effects or in neutron capture therapy). Suitable Bemitting ions are, for example S, 7 cSc, "Ga, "Ga and 0

Y.

Suitable -emittinion exhibitig short half-lives are, for Suitable &-emittinglon6' exhibiting short half-lives are, for Z W "MI! example, 211 Bi, 21 2 Bi, 213 Bi and 214 Bi, whereby 212 Bi is preferred. A suitable photon- and electron-emitting ion is 158 Gd, which can be obtained from 157Gd by neutron capture.

If the agent according to the invention is intended for use in the variant of radiation therapy proposed by R. L. Mills et al. (Nature Vol. 336, (1988), p. 787), the central ion must be derived from a M~ssbauer isotope, such as, for example, 5 Fe or 151 Eu.

In the in vivo administration of the therapeutic agents according to the invention, the latter can be administered together with a suitable vehicle, such as, for example, serum, or physiological common salt solution and together with another protein, such as, for example, human serum albumin. In this case, the dosage depends on the type of cellular disorder, the metal ion used and the type of imaging method.

The therapeutic agents according to the invention are 0.0. administered parenterally, preferably i.v.

Details of use of radiotherapeutic agents are discussed in, R. W. Kozak et al. TIBTEC, October 1986, 262.

:00"0: The agents according to the invention are extremely well suited as x-ray contrast media, whereby it is especially to be emphasized that no signs of the anaphylaxis-like reactions, known from the iodine-containing contrast media, can be detected with them in biochemical-pharmacological studies. They are especially valuable because of the advantageous absorption properties in the areas of higher tube voltages for digital subtraction techniques.

In general, the agents according to the invention are dosed for use as x-ray contrast media analogously to, for example, meglumine-diatrizoate in amounts of 0.1-5 mmol/kg, preferably 0.25-1 mmol/kg.

Details of use of x-ray contrast media are discussed in, for example, Barke, R8ntgenkontrastmittel [X-Ray Contrast Media], G.

Thieme, Leipzig (1970) and P. Thurn, E. BUcheler "EinfUhrung in die R8ntgendiagnostik [Introduction to Diagnostic Radiology]," G. Thieme, Stuttgart, New York (1977).

In general, it has been possible to synthesize new complexing agents, metal complexes and metal complex salts, which open up new possibilities in diagnostic and therapeutic medicine.

The following examples are used for a more detailed explanation of the object of the invention: 54 Example 1 a) 1,4,7-Tris(N,N'-dibenzyloxycarbonyl-lysyl) 4,7jO10tetraazacyclododecane 49.07 g (95.9 mmol) of di-Z-lysine-N-hydroxysuccinimide ester and 5 g (29 mmol) of cyclene (=1,4,7,10tetraazacyclododecane) are dissolved in a mixture of 200 ml of toluene/100 ml of dioxane. 9.7 g (95.9 mmol) of triethylamine is added and heated for 12 hours to 70 0 C. It is evaporated to the dry state, the residue is taken up in 600 ml of dichloromethane and extracted 3 times with 200 ml of 5% aqueous potassium carbonate solution each. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: ethyl acetate/ethanol 15:1).

Yield: 29.61 g (75% of theory) of a colorless solid Cld: C 65.28 H 6.81 N 10.29 Fnd: C 65.41 H 6.97 N 10.10 b) 1-(Carboxymethoxyacetyl)-4,7,10-tris(N,N'dibenzyloxycarbonyl-lysyl)-1,4,7,10-tetraazacyclododecane 3.58 g (30.86 mmol) of diglycolic acid anhydride and 6.24 g (61.72 mmol) of triethylamine are added to 28 g (20.56 mmol) of the title compound of Example a (dissolved in 200 ml of tetrahydrofuran). It is heated for 6 hours to 50 0 C. The solution is evaporated to the dry state in a vacuum, taken up with 300 ml of dichloromethane and extracted twice with 150 ml of SX -S ~r'M yi -f aqueous hydrochloric acid each. The organic phase is dried on magnesium sulfate, evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/methanol 20:1).

Yield: 27.65 g (91% of theory) of a colorless solid Elementary analysis: Cld: C 63.40 H 6.55 N 9.48 Fnd: C 63.21 H 6.70 N 9.27 Sc) 4 -Nitrophenoxy)-3-oxaglutaryl]-4,7,10-tris(N,N'dibenzyloxycarbonyl-lysyl)-1,4,7,10-tetraazacyclododecane 14.78 g (10 mmol) of the carboxylic acid described in Example 1b, dissolved in 150 ml of dichloromethane, is mixed first with 1.53 g (11 mmol) of 4-nitrophenol and then at OC with 2.27 g (11 mmol) of dicyclohexylcarbodiimide. After stirring overnight at room temperature, dicyclohexylurea is suctioned out, S the filtrate is concentrated by evaporation and reprecipitated from isopropanol. The mother liquor is decanted from the oily product that accumulates, the oil is taken up in dichloromethane and concentrated by evaporation in a vacuum. 15.4 g of foamy, solidified solid is obtained.

Elementary analysis: Cld: C 63.11 H 6.24 N 9.64 Fnd: C 62.98 H 6.31 N 9.80 -Iplrir--i 1F-.ir-- -'U0 d) Bis(2-(benzyloxycarbonylamino).-ethyl]-amine 51.5 g (500 mmol) of diethylenetriamine and 139 ml (1 mel) of triethylamine are dissolved in dichloromethane and mixed at -200C with 161 g of benzyl cyanoformate (Fluka) in dichloromethane and then stirred overnight at room temperature.

After the reaction is: completed, concentration by evaporation is performed during dra -fthe residue is taken up in diethyl ether, the organic -phas,. ais washed with sodium carbonate solution and dried with sodium sulfatei The filtrate is mixed with hexane, the precipitate ,Is filtered off and dried.

Yield: 163.4_ g;(88of theory) Elementary analysis: Cld: C 64.67 H 6.78 N 11.31 SFnd: C 64.58 H 6.83 N 11.28 e) N,N,N',N',N",N"-Hexakis[2-(benzyloxycarbonylamino)-ethyl]trimesic acid triamide 13.27 g (50 mmol) of .trimesic acid trichloride (Aldrich) and 34.7 ml (250 mmol) of triethylamine are dissolved in dimethylformamide (DMF) and mixed at OoC with 65.0 g (175 mmol) of the amine that is described in Example id and then stirred overnight at room temperature. The solution is concentrated by evaporation in a vacuum, and the residue is chromatographed on silica gel with ethyl acetate.

Yield: 39.4 g (62 oftheory) 1W Elementary analysis: Cld: C 65.24 H 5.95 N 9.92 Fnd: C 65.54 H 5.95 N 9.87 f) Completely protected benzyloxycarbonyl-36mer-polyamine, synthesized from N,N,N',N',N",N"-hexakis(2-aminoethyl)trimesic acid triamide-core and six amine-protected hexaamine-monocarboxylic acids that are described in Example lb 1.27 g (1 mmol) of the hexa-benzyloxycarbonylamine described ~i in Example J& is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred.

After 60 minutes, the incipient precipitation is completed with diethyl ether, the hexa-amine-hydrobromide produced is washed S with ether, dried in a vacuum and further reacted without further purification.

Yield: 0.95 g (quantitative) Then, the hexa-amine-hydrobromide is dissolved in 150 ml of :DMF, mixed with 15.99 g (10 mmol) of the 4-nitrophenyl-activated ester described in Example ic and with 4.05 g (40 mmol) of triethylamine, stirred overnight at room temperature and ultimately evaporated to the dry state in a vacuum. The residue is taken up in ethyl acetate and washed in succession with water, dilute sodium hydroxide solution and saturated NaCl solution.

The organic phase is dried on sodium sulfate, and the filtrate is -rri tS tZ LA'.?t Zr; r W evaporated to the dry state, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/methanol 18:2).

Yield: 6.55 g (71% of theory) of a colorless solid Elementary analysis: Cld: C 63.68 H 6.59 N 10.48 Fnd: C 63.83 H 6.70 N 10.29 MALDI-TOF mass spectrum: molar peak at 9246 (M Na*) i* g) 1-(Benzyloxycarbonylmethyl)-4,7,10-tris(tertbutoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane (as sodium bromide complex) g (38.87 mmol) of 1,4,7-tris(tert-butoxy-carbonylmethyl)- 1,4, 7 ,10-tetraazacyclododecane (D03A-tris-tert-butyl ester, produced according to EP 0 299 795, Example 22a, is dissolved in 100 ml of acetonitrile. Then, 11.45 g (50 mmol) of bromoacetic acid benzyl ester and 10.6 g (100 mmol) of sodium carbonate are added and stirred for 12 hours at 60 0 C. The salts are filtered out, the filtrate is evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: methylene chloride/methanol 20:1).

Yield: 21.72 g (73% of theory) of a colorless amorphous powder I Elementary analysis: Cld: C 54.90 H 7.63 N 7.32 Na 3.00 Br 10.44 Fnd: C 54.80 H 7.72 N 7.21 Na 2.89 Br 10.27 h) 1-(Carboxymethyl)-4,7,10-tris(tert-butoxycarbonylmethyl)- 1, 4 ,7,10-tetraazacyclododecane (as sodium bromide complex) g (26.12 mmol) of the title compound of Example lg is dissolved in 300 ml of isopropanol, and 3 g of palladium catalyst Pd/C) is added. It is hydrogenated overnight at room temperature. The catalyst is filtered out, and the filtrate is i evaporated to the dry state.

Yield: 17.47 g (99% of theory) of a colorless amorphous powder Elementary analysis: Cld: C 49.78 H 7.76 N 8.29 Na 4.44 Br 11.83 Fnd: C 49.59 H 7.59 N 8.17 Na 4.40 Br 11.70 i) 1-(4-Carboxy-2-oxo-3-azabutyl)-4,7,10-tris(tertbutoxycarbonylmethyl) l0-tetraazacyclododecane 1.73 g (15 mmol) of N-hydroxysuccinimide is added to 10 g (14.80 mmol) of the title compound of Example lh in 100 ml of dimethylformamide and cooled to 0°C. Then, 4.13 g (20 mmol) of dicyclohexylcarbodiimide is added and stirred for 1 hour at 0°C and then for 2 hours at room temperature. It is cooled to o0C, and then 5.1 g (50 mmol) of triethylamine and 2.25 g (30 mmol) of glycine are added. It is stirred overnight at room temperature.

Precipitated urea is filtered out, and the filtrate is evaporated to the dry state in a vacuum. The residue is taken up with water and extracted twice with methylene chloride. The organic phase is dried on magnesium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel (mobile solvent: methylene chloride/methanol 15:1).

Yield: 8.20 g (88% of theory) of a colorless solid Elementary analysis: Cld: C 57.21 H 8.80 N 11.12 .oo. Fnd: C 57.10 H 8.91 N 11.03 k) 36 mer-N-(5-DO3A-yl-4-oxo-3-azapentanoyl)-cascade polyamide based on the 36mer-polyamine described in Example If [DO3A l,4,7-tris(carboxymethyl)-l,4,7,10tetraazacyclododecane] 1.84 (0.2 mmol) of the 36mer-benzyloxycarbonylamine described in Example 11 is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide produced is washed with ether, dried in a vacuum and used without further purification in the reaction further described below.

Yield: 1.5 g (quantitative) 14.7 g (20 mmol) of the carboxylic acid described in Example 1L, 3.0 g (20 mmol) of 1-hydroxybenzotriazole and 6.4 g (20 mmol) .V .SS ThVA P A.

of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl-uronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15 minutes. The solution is then mixed with 10.3 ml (60 mmol) of N-ethyldiisopropylamine and with 1.5 g (0.2 mmol) of the above-described 36mer-amine-hydrobromide and stirred for 4 days at room temperature. After the reaction is completed, it is concentrated by evaporationi in.a vacuum, the residue is dissolved at 0°C in trifluoroacetilcacid, stirred overnight at room temperature, concentrated by evaporation in a vacuum, and the residue is stirred with ether. The substance is suctioned off, washed with ether,' ,dried in a vacuum, ultimately dissolved in u l t i m at d i n S water, set at pH 7 with 2N sodium hydroxide solution, and the solution is purified with an Amicona)-ultrafiltration membrane YM3 (cut off: 3000 Da). The retentate is then filtered and freeze-dried.

Yield: 3.61 g (72% of theory) of a flocculent powder H. O content (Karl-Fischer): 8.9% Elementary analysis (relative to anhydrous substance): Cld: C 44.86 H 5.87 N 15.34 Na 10.92 Fnd: C 45.09 H 5.80 N 15.44 Na 10.51 1) 36mer-Gd Complex of the ligand described in the example above g (0.1 mmol) of the sodium salt of the complexing agent acid described in Example 1k) above is acidified in water with ml of glacial acetic6acid, mixed with 725 mg (2 mmol) of Gd 2 O l, z~ and complexed for 2 hours at 80 0 C. After cooling, the solution is filtered, the filtrate is ultrafiltered with YM3 (AMICON(R'), and the retentate is set at minimum conductivity by alternately adding cation exchanger IR 120 form) and anion exchanger IRA 410 (OH' form). Exchanger is filtered out, and the filtrate is freeze-dried.

Yield: 1.96 g (70% of theory) of a colorless, flocculent powder H.O content (Karl-Fischer): 7.4% Gd determination (AAS): 19.9% MALDI-TOF mass spectrum: molar peak at 25,905 Da (Cld: 25,911 Da) Elementary analysis (relative to anhydrous substance): Cld: C 39.35 H 5.15 Gd 21.85 N 13.46 Fnd: C 39.08 H 5.29 Gd 21.03 N 13.68 o T,-relaxivity (H 2 18.0 0.2 (1/mmol sec) (plasma): 21.5 0.5 (1/mmol sec) Total-body-retention after intravenous administration (0.1 mmol of gadolinium/kg of body weight; after 14 days; rats): 1.09 0.17% of the dose.

The corresponding europium complex showed the following values: Rabbit: 0.23 0.12% of the dose Mouse: 0.46 0.1% of the dose Bxample 2 a) 2-Bromopropionylglycine-benzyl ester 55.9 g (326.1 mmol) of 2-bromopropionic acid chloride is added in drops at 0 C to 100 g (296.4 mmol) of glycine benzyl ester-p-toluenesulfonic acid salt and 33.0 g (326.1 mmol) of triethylamine in 400 ml of methylene chloride. The temperature is not allowed to exceed 5 0 C. After addition is completed, it is stirred for 1 hour at 0 C, then for 2 hours at room temperature.

500 ml of ice water is added, and the aqueous phase is set at pH S 2 with 10% aqueous hydrochloric acid. The organic phase is separated, washed once with 300 ml of 5% aqueous soda solution and 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is recrystallized from diisopropyl ether.

s.

Yield: 68.51 g (75% of theory) of a colorless crystalline powder Elementary analysis: Cld: C 46.76 H 7.19 N 4.54 Br 25.92 Fnd: C 46.91 H 7.28 N 4.45 Br 25.81 b) 1-[4-(Benzyloxycarbonyl)-l-methyl-2-oxo-3-azabutyl]- 1,4,7,10-tetraazacyclododecane g (162.2 mmol) of the title compound of Example 2a is added to 55.8 g (324.4 mmol) of 1, 4 ,7,10-tetraazacyclododecane, dissolved in 600 ml of chloroform, and stirred overnight at room temperature. 500 ml of water is added, the organic phase is i ,v separated and washed twice each with 400 ml of water. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: chloroform/methanol/aqueous 25% ammonia 10:5:1).

Yield: 40.0 g (63% of theory relative to the 2a used) of a slightly yellowish viscous oil Elementary analysis: Cld: C 61.36 H 8.50 N 17.89 Fnd: C 61.54 H 8.68 N 17.68 S c) 1-[4-(Benzyloxycarbonyl)-l-methyl-2-oxo-3-azabutyl]-4,7,10- .*tris(tert-butoxycarbonylmethyl)-1,4,7,10tetraazacyclododecane (sodium bromide complex) 33 g (169 mmol) of bromoacetic acid-tert-butyl ester is added to 20 g (51.08 mmol) of the title compound of Example 2b and 17.91 (169 mmol) of sodium carbonate in 300 ml of acetonitrile, and it is stirred for 24 hours at 60 0 C. It is cooled to 0 C, the salts are filtered out, and the filtrate is evaporated to the dry state. The residue is chromatographed on S silica gel (mobile solvent: ethyl acetate/ethanol: 15:1). The fractions that contain the product are concentrated by evaporation, and the residue recrystallizes from diisopropyl ether.

Yield: 34.62 g (81% of theory) of a colorless crystalline powder l w Elementary analysis: Cld: C 54.54 H 7.59 N 8.37 Na 2.74 Br 9.56 Fnd: C 54.70 H 7.65 N 8.24 Na 2.60 Br 9.37 d) 1-(4-Carboxy-l-methyl-2-oxo-3-azabutyl)-4,7,10-tris(tertbutoxycarbonylmethyl)-1,4,7,10 O-tetraazacyclododecane (sodium bromide complex) g (35.85 mmol) of the title compound of Example -2 is dissolved in 500 ml of isopropanol, and 3 g of palladium catalyst Pd/C) is added. It is hydrogenated overnight at room temperature. Catalyst is filtered out, the filtrate is evaporated to the dry state in a vacuum and recrystallized from acetone.

Yield: 22.75 g.(85% of theory) of a colorless crystalline powder Elementary analysis: Cld: C 49.86 H 7.69 N 9.38 Na 3.07 Br 10.71 Fnd: C 49.75 H 7.81 N 9.25 Na 2.94 Brl10.58 0 e) 1-[4-(4-Nitrophenoxycarbonyl)-1-methyl-2-oxo-3-azabutyl]- 4,7,1 0-tris(tert-butoxy-carbonylmethyl)-1,4,7,10tetraazacyclododecane (sodium bromide complex) 37.3 g (50 mmol) of the carboxylic acid described in Example 2d above is mixed in 500 ml of dichloromethane with 7.6 g mmol) of 4-nitrophenol and cooled to 0 0 C. After adding 10.8 g (52.5 mmol) of dicyclohexylcarbodiimide, it is stirred overnight j~i 66 at room temperature, then precipitated dicyclohexylurea is suctioned out with renewed cooling, and the filtrate is evaporated to the dry state in a vacuum. The residue is recrystallized from ethyl acetate.

Yield: 40.3 g.(92.9% of theory) of a slightly yellowish powder Elementary analysis: Cld: C 51.21 H 6.97 N 9.68 Na 2.65 Br 9.21 Fnd: C 51.06'- Hi7 .07 N 9.82 Na 2.40 Br 8.77 f) 36mer-N-(5-DO3A-yl-4-oxo-3-azahexanoyl) -cascade polyamide based on the 36mer-polyamine described in Example If 1.84 g (0.2 amol) of the 36mer-benzyloxycarbonylamine described in Example 1i is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide produced is washed with ether, dried in a vacuum and reacted without further purification.

Yield: 1.5 g (quantitative) g of the above-described 36mer amine-hydrobromide in 100 ml of DMF is mixed with 17.4 g (20 mmol) of the p-nitrophenylactivated ester described in Example 2e. Within one hour, a solution of 5.05 g, (50 mmol) of triethylamine in 20 ml of DMF is then slowly added in drops, so that the precipitate forming at t i 67 the beginning can again dissolve. It is stirred overnight at 450C, then the solution is concentrated by evaporation in a vacuum, the residue is dissolved at OOC in trifluoroacetic acid and stirred overnight at room temperature. It is concentrated by evaporation in a vacuum, the residue is stirred with diethyl ether, the precipitate is suctioned off and dried in a vacuum.

The acidic crude product is ultimately dissolved in water, set at pH 7 with dilute sodium hydroxide solution and'ultrafiltered with an AMICON"R YM-3 membrane. The retentate is freeze-dried.

Yield: 4.0 g (78% of theory)

H

2 0 content (Karl-Fischer): 9.3% Elementary analysis (relative to anhydrous substance): Cld: C 45.74 H 6.05 N 15.01 Na 10.68 Fnd: C 45.84 H 5.93 N 15.22 Na 10.20 g) 36mer-Gd Complex of the ligand described in the example above 2.5 g (0.1 mmol) of the sodium salt of the complexing agent acid described in Example 2f above is acidified in water with ml of glacial acetic acid, mixed with 725 mg (2 mmol) of GdO 3 and complexed for 2 hours at 80 0 C. After cooling, the solution is filtered, the filtrate is ultrafiltered with YM3 (AMICON)), and the retentate is set at minimum conductivity by alternately adding cation exchanger IR 120 form) and anion exchanger IRA 410 (OH- form). Exchanger is filtered out, and the filtrate is freeze-dried.

*'sss~m' Va Yield: 2.14 g (74% of theory) of a colorless, flocculent powder

H

2 0 content (Karl-Fischer): 8.7% Gd determination (AAS): 19.4% MALDI-TOF mass spectrum: molar peak at 26,426 Da (Cld: 26,416 Da) Elementary analysis (relative to anhydrous substance): Cld: C 40.24 H 5.32 Gd 21.43 N 13.20 Fnd: C 39.97 H 5.50 Gd 21.19 N 13.32 TI -relaxivity (H 2 17.5 0.1 (1/iumol sec) :(plasma): 18.2 ±0.2 (1/mmol sec) :Total-body-retention after intravenous administration (0.1 mmol of gadolinium/kg of body weight; after 14,days; rats): 1.74 ±0.22% of the dose.

The corresponding europium complex showed the following 99~ values: Rabbit: 0.32 ±0.16% of the dose Mouse: 1.0 of the dose Example 3 1,4,7-Tris(N-benzyloxycarbonylglycyl).1,4,7,10tetraazacyclododecane 29.37 g (95.9 mmol) of Z-glycirle-N-hydroxysuccinimide ester and 5 g (29 mmol) of cyclene (=1,4,7,10-tetraazacyclododecane) 69 are dissolved in a mixture of 100 ml of toluene/50 ml of dioxane.

9.7 g (95.9 mmol) of triethylamine is added and heated for 12 hours to 70°C. It is evaporated to the dry state, the residue is taken up in 400 ml of dichloromethane and extracted 3 times with 200 ml of 5% aqueous potassium carbonate solution each. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: ethyl acetate/ethanol 15:1).

Yield: 17.52 g (81% of theory) of a colorless solid Elementary analysis: Cld: C 61.20 H 6.35 N 13.15 Fnd: C 61.07 H 6.45 N 13.01 b) 1-(Carboxymethoxyacetyl)-4,7,10-tris(Nbenzyloxycarbonylglycyl)-1,4,7,10-tetraazacyclododecane 3.97 g (34.19 mmol) of diglycolic acid anhydride and 6.92 g (68.38 mmol) of triethylamine are added to 17 g (22.79 mmol) of the title compound of Example 3a (dissolved in 100 ml of tetrahydrofuran). It is heated for 6 hours to 50°C. The solution is evaporated to the dry state in a vacuum, taken up with 250 ml of dichloromethane and extracted twice with 100 ml of aqueous hydrochloric acid each. The organic phase is dried on magnesium sulfate, evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/methanol 20:1).

Yield: 17.48 g (89% of theory) of a colorless solid Elementary analysis: Cld: C 58.53 H 5.96 N 11.38 Fnd: C 58.37 H 5.81 N 11.45 c) Bis(2-(N,,N -dibenzyloxycarbonyl-lysylamino)-ethyl]-amine 1.03 g (10 mmol) of diethylenetriamine is dissolved in 100 ml of THF, mixed with 2.02 g (2.77 ml, 20 umol) of triethylamine and 11.25 g (21 mmol) of N,N'-di-benzyloxycarbonyl-lysine-pnitro-phenylester W. Lever et al., J. Heterocyclic Chem., 2a, 901 903 (1986)] and stirred for 3 hours at room temperature.

The thick suspension produced is made up with ether to 250 ml, stirred overnight at room temperature, the voluminous precipitate is suctioned off and washed with 100 ml of THF/ether and then again with ether. After drying in a vacuum at 40 0 C, 8.7 g (97.1% of theory) of a colorless powder is obtained.

Elementary analysis: Cld: C 64.34 H 6.86 N 10.94 Fnd: C 64.20 H 6.97 N 10.81 d) N,N,N',N',N",N"-Hexakis[2-(N 6 ,N -dibenzyloxycarbonyllysylamino)-ethyl]-trimesic acid triamide 1.43 g (1.6 mmol) of bis[2-(N., N-dibenzyloxycarbonyllysylamino)-ethyl]-amine in 20 ml of DMF is mixed at OOC with 1.39 ml (1.01 g, 10 mmol) of triethylamine and 0.11 g (0.4 mmol) of trimesic acid trichloride (Aldrich) and stirred for 2 hours in ice and overnight at room temperature. It is then concentrated by evaporation in a vacuum, taken up in ethyl acetate and washed A- m with dilute sodium hydroxide solution, 1 M hydrochloric acid and semi-saturated NaCl solution and dried on sodium sulfate. After activated carbon is added, it is filtered out with a teflon membrane filter, the filtrate is concentrated by evaporation dissolved again in about 5 ml of ethyl acetate and chromatographed on silica gel with ethyl acetate/methanol (18:2).

Yield: 0.9 g (79 it of a colorless powder Elementary analysis:i Cld: C 64.61 H 6.48 N 10.34 Fnd: C 64.45 H 6.60 N 10.28 e) Completely protected benzyloxycarbonyl-36mer-polyamine, synthesized from N. N, Ni' ,N",N"-hexakis 2-(lysylamino)- S. ethyl]-trimesic acid-triamide-core and twelve amineprotected triamine-monocarboxylic acids described in Example 3b 2.84 g (1 mmol) of the 1 2 mer-benzyloxycarbonylamine described in Example ad above is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 3 hours, the incipient precipitation is completed with diethyl ether, the 12mer-amine-hydrobromide produced is washed with ether, dried in a vacuum, and used without further purification in the reaction further described below.

Yield: 2.2 g (quantitative) s~~-tw F-sF i'~w 17.2 g (20 mmol) of the cyclene-carboxylic acid described in Example 3b, 3.0 g (20 mmol) of 1-hydroxybenzotriazole and 6.4 g mmol) of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl-uronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15 minutes. The solution is then mixed with 10.3 ml (60 mmol) of N-ethyldiisopropylamine and with 2.2 g (1 mmol) of the above-described 12mer-amine-hydrobromide and stirred overnight at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, and the residue is chromatographed on silica gel with dichloromethane/methanol (17:3).

Yield: 9.6 g (84.5% of theory) of a colorless powder .e Elementary analysis: Cld: C 59.31 H 6.20 N 12.94 Fnd: C 59.20 H 6.03 N 13.19 ooo.

MALDI-TOF mass spectrum: molar peak at 11,384 (M+Na+) f) 36mer-N-(5-DO 3 A-yl-4-oxo-3-azapentanoyl)-cascade polyamide based on the 36mer polyamine described in Example 3e 2.27 (0.2 mmol) of the 3 6 mer-benzyloxycarbonylamine described in Example 3e is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide 1 -r-itr~r~ produced is washed with ether, dried in a vacuum and used without further purification in the reaction further described below.

Yield: 1.9 g (quantitative) 14.7 g (20 mmol) of the carboxylic acid described in Example li, 3.0 g (20 mmol) of 1-hydroxybenzotriazole and 6.4 g (20 mmol) of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15 minutes. The solution is then mixed with 10.3 ml (60 mmol) of N-ethyldiisopropylamine and with 1.9 g (0.2 mmol) of the above-described 36mer-amine-hydrobromide and stirred for 4 days at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, the residue is dissolved at 0

O

C in trifluoroacetic acid, stirred overnight at room temperature, concentrated by evaporation in a vacuum, and the residue is stirred with ether. The substance is suctioned off, washed with ether, dried in a vacuum, ultimately dissolved in water, set at pH 7 with 2N sodium hydroxide solution, and the solution is purified with an AmiconCR)-ultrafiltration membrane YM 3 (cut off: 3000 Da). The retentate is then filtered and freeze-dried.

Yield: 3.93 g (75% of theory) of a flocculent powder content (Karl-Fischer): Elementary analysis (relative to anhydrous substance): Cld: C 44.48 H 5.75 N 16.05 Na 9.98 Fnd: C 44.77 H 5.91 N 15.96 Na 9.50 g) 36mer-Gd Complex of the ligand described in Example 3f above 2.6 g (0.1 mmol) of the sodium salt of the complexing agent acid described in Example 3f above is acidified in water with ml of glacial acetic acid, mixed with 725 mg (2 mmol) of Gd 2 0 3 and complexed for 2 hours at 80°C. After cooling, the solution is filtered, the filtrate is ultrafiltered with YM3 (AMICON(R)), and the retentate is set at minimum conductivity by alternately adding cation exchanger IR 120 form) and anion exchanger IRA 410 (OH' form). Exchanger is filtered out, and the filtrate is freeze-dried.

Yield: 2.22 g (72% of theory) of a colorless, flocculent powder content (Karl-Fischer): 8.9% Gd determination (AAS): 18.5% MALDI-TOF mass spectrum: molar peak at 28,058 Da (Cld: 28,049 Da) Elementary analysis (relative to anhydrous substance): Cld: C 39.44 H 5.10 Gd 20.18 N 14.23 SFnd: C 39.56 H 5.26 Gd 19.88 N 14.09 Example 4 a) 36mer-N-(5-DO 3 A-yl-4-oxo-3-azahexanoyl)-cascade polyamide based on the 36mer polyamine described in Example 3e 2.27 g (0.2 mmol) of the 3 6 mer-benzyloxycarbonylamine described in Example 3e is dissolved in glacial acetic acid and evs' vs Wnr4r~x<5st mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide produced is washed with ether, dried in a vacuum and further reacted without further purification.

Yield: 1.9 g (quantitative) 1.9 g of the above-described 36mer amine-hydrobromide in 100 ml of DMF is mixed with 17.4 g (20 mmol) of the p-nitrophenylactivated ester described in Example 2e. Within one hour, a solution of 5.05 g (50 mmol) of triethylamine in 20 ml of DMF is then slowly added in drops, so that the precipitate forming at the beginning can again dissolve. It is stirred overnight at 450C, then the solution is concentrated by evaporation in a oo vacuum, the residue is dissolved at O

O

C in trifluoroacetic acid and stirred overnight at room temperature. It is concentrated by evaporation in a vacuum, the residue is stirred with diethyl ether, the precipitate is suctioned off and dried in a vacuum.

The acidic crude product is ultimately dissolved in water, set at pH 7 with dilute sodium hydroxide solution and ultrafiltered with an AMICON(R) YM-3 membrane. The retentate is freeze-dried.

o Yield: 4.0 g (72.9% of theory)

H

2 O content (Karl-Fischer): Elementary analysis (relative to anhydrous substance): Cld: C 45.30 H 5.92 N 15.73 Na 9.78 Fnd: C 45.56 H 6.10 N 15.65 Na 9.47 Ma I W b) 36mer-Gd Complex of the ligand described in Example AA above 2.74 g (0.1 mmol) of-the sodium salt of the complexing agent acid described in Example Aft above is acidified in water with al of glacial acetic acid, mixed with 725 mg (2 mmol) of Gd 2

O

3 and complexed for 2 hours at 8 0 0C. After cooling, the solution is filtered, the filtrate' is ultrafiltered with YM3 (AMICON()), and the retentat. is se tmnmmconductivity by alternately adding cation exchangerIR 1!k-20 form) and anion exchanger

IRA

4 10 (OH- form). Exchanpgerisfiltered out, and the filtrate is freeze-dried.

Yield: 2.46.%g (77.8% of'f theory) of a colorless, flocculent powder H.0 content (Karl-Fischer): .9.7% Gd determination, HALDI-TOF mass spectrum:. molar peak at 28,563 Da (Cld: 28,554 Da) Elementary analysis (relative to anhydrous substance): .Cld: C 40.26 H.5.26 Gd 19.83 N 13.98 Fnd: C 40.01 H 5.40. Gd 19.68 N 14.11 Example a) 1, 7-Bis (benzyloxycarbonyl) -4-kydroxysuccinyl-1,4,7triazaheptane 20.20 g (201.9 mmol) of succinic acid anhydride and 40.86 g (403.8 mmol) of triethl aii~e'iake added to 50 g (134.6 mmol) of 1, 7-bis (benzyloxycarbonyl) 7-triazaheptane (Example 1d) in 500 ml of tetrahydrofuran and stirred overnight at 40 0 C. It is evaporated to the dry state, the residue is taken up in 1,000 ml of dichloromethane and washed twice with 500 ml of hydrochloric acid each. The organic phase is dried on magnesium sulfate and evaporated to the dry state. The residue is chromatographed on silica gel (mobile solvent dichloromethane/methanol: 20:1).

Yield: 56.0 g (93% of theory) of a colorless solid Elementary analysis: Cld: C 59.05 H 6.53 N 9.39 Fnd: C 59.17 H 6.69 N 9.27 b) N-Hydroxysuccinimide ester of 1,7-bis(benzyloxycarbonyl)-4hydroxysuccinyl-1, 4,7-triazaheptane 14.4 g (125.14 mmol) of N-hydroxysuccinimide is added to 56 g (125.14 mmol) of the title compound of Example 5a in 300 ml of dichloromethane. It is cooled to 0°C, and 28.4 g (137.66 nmmol) of dicyclohexylcarbodiimide is added. Then, it is stirred for 6 hours at room temperature. Precipitated solid is filtered out, and the filtrate is evaporated to the dry state in a vacuum.

The residue is recrystallized from ether/2-propanol.

Yield: 62.01 g (91% of theory) of a crystalline colorless solid li i Ulr I. i I 7~ Elementary analysis: Cld: C 57.35 H 5.92 N 10.29 Fnd: C 57.24 H 5.99 N 10.12 c) 1,4,7-Tris{7-benzyloxycarbonylamino-5-[2azaheptanoyl} 1,4,7,10-tetraazacyclododecane 52.22 g (95.9 mmol) of the title compound of Example 5b and g (29 mmol) of cyclene 4 ,7,10-tetraazacyclododecane) are dissolved in a mixture of 200 ml of toluene/100 ml of dioxane.

9.7 g (95.9 mmol) of triethylamine is added and heated for 12 hours to 70 0 C. It is evaporated to the dry state, the residue is taken up in 600 ml of dichloromethane and extracted three times .oo. with 300 ml of 5% aqueous potassium carbonate solution each. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue is chromatographed on silica gel (mobile solvent: ethyl acetate/ethanol 15:1).

Yield: 28.95 g (69% of theory) of a colorless solid Elementary analysis: Cld: C 61.44 H 7.04 N 11.62 Fnd: C 61.57 H 6.91 N 11.69 7 7777 7 d) 1,4, 7 -Tris-7-benzyloxycarbonylamino5.2.

(benzyloxycarbonylamino) -ethyl) -4-oxo-5-azaheptanoyl}-1ohydroxysuccinyl-1, 4,7, 2.90 g (2.9 mmol) of succinic acid anhydride and 5.87 g (58 -mmol) of triethylamine are added'to 28 g (19.35 mmol) of the title compound of Example 5c, dissolved in tetrahydrofuran. It is heated for 6 hours to 50 0 C. The solution is evaporated to the dry state in a vacuum, taken up with 200 ml of dichloromethane and extracted twice with 100 ml of 5% aqueous hydrochloric acid I each. The organic phase is dried on magnesium sulfate, evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: 0. dichloromethane/methanol =20:1).

seesYield: 26.94 g (90% of theory) of a colorless solid Elementary analysis: s.

see* Cld: C 60.57 H 6.84 N 10.87 Fnd: C 60.41 H 6.95 N 10.75 sees e) 1,4,7,10,13, l 6 -Hexakis(N-benzyloxycarbonyl-B-alanyl].

1,4,7,10,13, 16-hexaazacyclooctadecane 0 S516 mg (2 mmol) of l, 4 ,7,lO,13,16-hexaazacyclooctadecane (hexacyclene; Fluka) is azeotropically dehydrated with toluene.

A solution of 3.35 g (15 mmol) of benzyloxycarbonyl-g-alanine (Sigma) in tetrahydrofuran (THF) as well as 3.71 g (15 mmol) of 2-ethoxy-1-ethoxcycarbonyl-1, 2-dihydroquinoline (EEDQ; Fluka) are added to the cooled solution of hexacyclene in toluene at room temperature and stirred overnight. After the reaction is completed, the product is precipitated by adding hexane, and the precipitate is chromatographed on silica gel with dichloromethane/hexane/isopropanol (20:10:1).

Yield: 2.06 g (69% of theory) Elementary analysis: Cld: C 62.89 H 6.50 N 11.28 Fnd: C 62.74 H 6.32 N 11.50 S f) Completely protected benzyloxycarbonyl-36mer-polyamine, :synthesized from 1,4,7,10,13,16-hexakis(B-alanyl)- 1,4,7,10,13, 16 -hexaazacyclooctadecane-core and six amineprotected hexaamine-monocarboxylic acids described in Example 1.49 g (1 mmol) of the hexa-benzyloxycarbonylamine described in Example 5e above is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 60 minutes, the incipient precipitation is completed with diethyl ether, the hexamine-hydrobromide produced is washed with ether, dried in a vacuum and used without further purification in the reaction further described below.

Yield: 1.2 g (quantitative) g (7.5 mmol) of the amine-protected hexa-aminemonocarboxylic acid described in Example 5d, 1.2 g (7.5 mmol) of 1-hydroxybenzotriazole and 2.4 g (7.5 mmol) of 2-(1H- I. benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for minutes. This solution is then mixed with 5.16 ml (30 amol) of N-ethyldiisopropylamine and with 1.2 g (1 mmol) of the abovedescribed hexa-amine-hydrobromide and stirred overnight at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum ai; the residue is chromatographed on silica gel with dichlorme thanemethanol (17:3).

Yield: 8.5 g (82% of theory) of a colorless powder Elementary analysis:' Cld: C 61.83. H 6.59 N 12.15 Fnd: C 61.59, H 6.71. N 12.02 MALDI-TOF mass spectrum: molar peak at 10.397 (M+Na) g) 36mer-N-(5-DO3A-yl-4-oxo-3-azahexanoyl)-cascade polyamide based on the polyamine described in Example 2.07 g (0.2 amol) of the 36mer-benzyloxycarbonylamine described in Example Ut is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide produced is washed with ether and dried in a vacuum and reacted without further purification.

Yield: 1.7 g (quantitativi) r V' X~Y2~4. 1.7 g of the above-described 36mer amine-hydrobromide in 100 ml of DMF is mixed with 17.4 g (20 mmol) of the p-nitrophenylactivated ester described in Example 2e. Within one hour, a solution of 5.05 g (50 mmol) of triethylamine in 20 ml of DMF is then slowly added in drops, so that the precipitate forming at the beginning can again dissolve. It is stirred overnight at 0 C, then the solution is concentrated by evaporation in a vacuum, the residue is dissolved at 0°C in trifluoroacetic acid and stirred overnight at room temperature. It is concentrated by evaporation in a vacuum, the residue is stirred with diethyl ether, the precipitate is suctioned off and dried in a vacuum.

o**oo* The acidic crude product is ultimately dissolved in water, set at pH 7 with dilute sodium hydroxide solution and ultrafiltered with an AMICONR) YM-3 membrane. The retentate is freeze-dried.

Yield: 4.4 g (83% of theory)

H

2 HO content (Karl-Fischer): 7.8% Elementary analysis (relative to anhydrous substance): Cld: C 45.80 H 6.08 N 15.51 Na 10.18 Fnd: C 45.88 H 6.23 N 15.66 Na 9.70 h) 36mer-Gd complex of the ligand described in Example 5g above 2.65 g (0.1 mmol) of the sodium salt of the complexing agent acid described in Example 5g above is acidified in water with ml of glacial acetic acid, mixed with 725 mg (2 mmol) of Gd 2 0 3 and complexed for 2 hours at 80°C. After cooling, the solution is filtered, the filtrate is ultrafiltered with YM3 (AMICON w and the retentate is set at minimum conductivity by alternately adding cation exchanger IR 120 form) and anion exchanger IRA 410 (OH" form). Exchanger is filtered out, and the filtrate is freeze-dried.

Yield: 2.41 g (81% of theory) of a colorless, flocculent powder

H

2 0 content (Karl-Fischer): Gd determination (AAS): 18.7% MALDI-TOF mass spectrum: molar peak at 27,580 Da (Cld: 27,566 Da) Elementary analysis (relative to anhydrous substance): Cld: C 40.52 H 5.37 Gd 20.54 N 13.72 Fnd: C 40.30 H 5.50 Gd 20.11 N 13.56 Example 6 36mer-Gd-DTPA-monoamide based on the 36mer-polyamine described in Example 1.04 g (0.2 mmol) of the 36 mner-poly-benzyloxycarbonylamine described in Example 5 is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 3 hours, the incipient precipitation is completed with diethyl ether, the 3 6 mer-amine-hydrobromide produced is washed with ether and dried in a vacuum. The residue is then taken up in water and set at pH 9.5 by adding 1N sodium hydroxide solution. 4.35 g (10.8 mmol) of N 3 dioxomorpholinoethyl)

-N

6 (ethoxycarbonylmethyl) -3,6diazaoctanedioic acid (Example 13a of EP 0331 616) is added in solid form to this solution, and the pH is kept constant at by further addition of sodium hydroxide solution. After the addition is completed, a pH 13 is set to saponify the DTPAethyl ester with 5N sodium hydroxide solution, and it is stirred overnight at room temperature. Then, it is set at pH 5 with concentrated hydrochloric acid, mixed with 1.96 g (5.4 mmol) of GdzO3, stirred for 30 minutes at 80°C, set at pH 7 after the cooling and desalted with a YM3 AMICON-ultrafiltration membrane.

The retentate is ultimately membrane-filtered and freeze-dried.

Yield: 2.58 g (92.4% of theory) HzO content (Karl-Fischer): Gd determination (AAS): 20.3% Elementary analysis (relative to anhydrous substance): Cld: C 35.46 H 4.26 Gd 22.29 N 10.92 Na 3.26 Fnd: C 35.18 H 4.44 Gd 21.75 N 10.83 Na 3.59 Example 7 a) 5-Benzyloxycarbonylamino-2-[3-(benzyloxycarbonylamino)propyl]-valeric acid 24.48 g (143.5 mmol) of benzyl chloroformate and 5N aqueous sodium hydroxide solution are simultaneously added in drops at 0°C to 10 g (57.39 mmol) of 4 -carboxy-1,7-diaminoheptane (produced according to: A. Reissert, Chem. Ber. 26, 2137 (1893); 22, 979 (1894)) in 150 ml of water, and the pH is kept at 10. It is stirred overnight at room temperature. It is extracted twice with 150 ml of ethyl acetate each. The aqueous phase is carefully acidified with 4N aqueous hydrochloric acid (pH 2) and extracted three times with 200 ml of ethyl acetate each. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum.

Yield: 24.13 g (95% of theory) of a vitreous solid Elementary analysis: Cld: C 59.05 H 6.53 N 9.39 Fnd: C 59.19 H 6.71 N 9.18 b) 5-Benzyloxycarbonylamino-2-[3-(benzyloxycarbonylamino)propyl]-valeric acid-N-hydroxysuccinimide ester 6.24 g (54.24 mmol) of N-hydroxysuccinimide is added to 24 g (54.24 mmol) of the title compound of Example 7a, dissolved in 100 ml of dichloromethane. It is cooled to 0°C, and 12.31 g (59.66 mmol) of dicyclohexylcarbodiimide is added. Then, it is stirred for 6 hours at room temperature. Precipitated solid is filtered out, and the filtrate is evaporated to the dry state in a vacuum. The residue is recrystallized from ether/2-propanol.

Yield: 27.51 g (94% of theory) of a crystalline, colorless solid Elementary analysis: Cld: C 62.33 H 6.16 N 7.79 Fnd: C 62.17 H 6.03 N 7.85 7il(r- -r~r i- y C) 1, 4 7 -Tris{5-benzyloxycarbonyla~ino-2. (3- (benzyloxycarbonylamino) -propyl ]-valeryl}-1, 4,7,10tetraazacyclododecane 27 g (50.04 mmol) of the title compound of Example 2, arnd 2.61 g (15.16 mmol) of cycloene (=l.4,7,lO-tetraazacyclododecane) are dissolved in a mixtureo 100 ml of toluene/50 ml of dioxane.

3.07 g (30.32 mmol).tgitri1thkline is added and heated for 12 hours to 700C. It is* -evapo rated to the dry state, the residue is taken up in 300 ml of dichloromethane and extracted three times! with 150 ml of 5% aqueous. potassum carbonate solution each. The organic phase is dried' on .magnesium sulfate and evaporated to the *dry state in-a vacuum. The residue is chromatographed on silica gel (mobile solvent: ethy acetate/ ethanol 15:1).

~Yield: 13. 81 g, of.. theory) of a colorless solid Elementary analysis: Cld: C 66.46 H 7.26 N 9.69 Fnd: C 66.28 H 7.39 N 9.51 d) l-(Carboxy-methoxyacetyl) 10-tris{5benzyloxycarb .orylamino- 2- 3-benzyloxycarbonylamino) -propyl] valerylj-1,4,7, l0-tetraazacyclododecane 1.57 g (13.5 mmol) -of diglycolic acid anhydride and 2.73 g (27 umol) of triethylamirie are added to 13 g (9 mmol) of the title compound of Example' Zc in 80 ral of tetrahydrofuran. It is heated for 6 hours to 50 0 The ~Solution is evaporated to the dry state in a vacuum,:taken up'with 150 ml of dichloromethane fAg- *.Zt~''fA&SfAVAg~ -Ag 87 and extracted twice with 100 ml of 5% aqueous hydrochloric acid each. The organic phase is dried on magnesium sulfate, evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/methanol 20:1).

Yield: 12.5 g (89% of theory) of a colorless solid Elementary analysis: Cld: C 64.60 H 6.97 N 8.97 Fnd: C 64.41 H 6.85 N 8.90 e) Completely protected benzyloxycarbonyl-36mer-polyamine, synthesized from N,N,N',N',N",N"-hexakis(2-aminoethyl)trimesic acid triamide-core and six amine-protected hexaamine-monocarboxylic acids described in Example 7d 1.27 g (1 mmol) of the hexa-benzyloxycarbonylamine described in Example le above is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 60 minutes, the incipient precipitation is completed with diethyl ether, the hexamine-hydrobromide produced is washed with ether, dried in a vacuum and used without further purification in the reaction further described below.

Yield: 0.95 g (quantitative) 11.7 g (7.5 mmol) of the cyclene-carboxylic acid described in Example 2d, 1.2 g (7.5 mmol) of 1-hydroxybenzotriazole and 2.4 g (7.5 mmol) of 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl- S~ 88 uronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15 minutes. This solution is then mixed with 5.16 ml (30 mmol) of N-ethyldiisopropylamine and with 0.95 g (1 mmol) of the above-described hexa-amine-hydrobromide and stirred overnight at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, and the residue is chromatographed on silica gel with dichloromethane/ methanol (17:3).

Yield: 7.40 g (76% of theory) of a colorless powder Elementary analysis: Cld: C 64.82 H 6.99 N 9.93 Fnd: C 64.58 H 7.11 N 10.04 MALDI-TOF mass spectrum: molar peak at 9751 (M+Na*) f) 36mer-N-(5-DO3A-yl-4-oxo-3-azahexanoyl)-cascade polyamide based on the polyamine described in Example 7e e 1.95 g (0.2 mmol) of the 36mer-benzyloxycarbonylamine described in Example 7e is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide produced is washed with ether and dried in a vacuum and reacted without further purification.

Yield: 1.6 g (quantitative) 1.6 g of the above-described 36mer amine-hydrobromide in 100 ml of DMF is mixed with 17.4 g (20 mmol) of the p-nitrophenylactivated ester described in Example 2e. Within one hour, a solution of 5.05 g (50 mmol) of triethylamine in 20 ml of DMF is then slowly added in drops so that precipitate forming at the beginning can again dissolve. It is stirred overnight at then the solution is concentrated by evaporation in a vacuum, the residue is dissolved at OOC in trifluoroacetic acid and stirred overnight at room temperature. It is concentrated by evaporation in a vacuum, the residue is stirred with diethyl ether, the precipitate is suctioned off and dried in a vacuum. The acidic crude product is ultimately dissolved in water, set at pH 7 with oo dilute sodium hydroxide solution and ultrafiltered with an AMICONR) YM-3 membrane. The retentate is freeze-dried.

Yield: 3.9 g (76% of theory)

H

2 0 content (Karl-Fischer): Elementary analysis (relative to anhydrous substance): Cld: C 46.59 H 6.23 N 14.69 Na 10.46 Fnd: C 46.82 H 6.47 N 14.55 Na 10.19 g) 36mer-Gd complex of the ligand described in the example above 2.58 g (0.1 mmol) of the sodium salt of the complexing agent acid described in Example 71 above is acidified in water with ml of glacial acetic acid, mixed with 725 mg (2 mmol) of GC 2

O

3 and complexed for 2 hours at 80°C. After cooling, the solution Th V-yc~V~V r2s~rSt is filtered, the filtrate is ultrafiltered with YM3 (AMICON M), and the retentate is set at minimum conductivity by alternately adding cation exchanger IR 120 form) and anion exchanger IRA 416~ (OH' f orm). Exchanger is f iltered out, and the f iltrate is freeze-dried.

Yield: 2.08 g (72% of theory) of a colorless, flocculent powder

H

2 0 conte nt (Karl-Fischer): Gd determination (AAS): 19.3% HALDI-TOF mass spectrum: molar peak at 26,915 Da (Cid: 26,921 Da) .Elementary analysis (relative to anhydrous substance): Cld: C 41.09 H 5.49 Gd 21.03 N-12.96 **Fnd: C 41.20 H 5.60 Gd 20.66 N 13.19 Example8 a) 3, 5-Bis[4-(benzyloxycarbonyl) -2-oxo-1, 4-diazabutyl]-benzoic acid 123.8 g (404.2 mmol) of N-Z-glycine-N-hydroxysuccinimide ester is added to 30 g (197.17 mmol) of 3,5-diaminobenzoic acid in 600 ml of dichloromethane. At 0 0 C, 60.7 g (800 inmol) of triethylanine, dissolved in 100 ml of dichloromethane, is added in drops within 5 minutes, and it is stirred overnight at room temperature. It is extracted three times with 500 ml of hydrochloric acid each, the organic phase is dried on magnesium C X~hr rC,-~X-CXscC$ 91 sulfate and evaporated to the dry state in a vacuum. The residue is recrystallized from acetone.

Yield: 97.87 g (95% of theory) of a colorless, crystalline solid Elementary analysis: Cld: C 59.77 H 5.02 N 10.72 Fnd: C 59.65- 5 .17 N 10.59 b) 3,5-Bis[4- (benzyloxycarbonyl-2-oxo-1,4-diazabutyl]-benzoic Sacid-N-hydroysuc"cinii id .ester 13.21 g (114.8 anol) of K-hydroxysuccinimide is added to g (114.8 mmol) of, the.titl compound of Example Sa, dissolved in 300 ml of dichloromethanel". .ItK is cooled to OOC, and 26.06 g (126.3 mmol) of dicyclohexylcarbodiimide is added. Then, it is stirred for 6 hours at room temperature. Precipitated solid is filtered out, and the filtrate is evaporated to the dry state in 0 a vacuum. The residue is recrystallized from ether/2-propanol.

Yield: 65.44 g (92% of theory) of a crystalline, colorless ~solid Elementary analysis: Cld: C 58.16 H 4072 N 11.30 Fnd: C 58.31 H 4.90 N 11.15 c) 1,4, 7 -Tris{3,5-bis-[4-benzylo xycarbonyl-2-oxo-1,4diazabutyl]-benzoyl}-1,4,7,10-tetraazacyclododecane g (96.84 mmol) of the title compound of Example 8b and 5.05 g (29.34 mmol) of cyclene (=1,4,7,10-tetraazacyclododecane) are dissolved in a mixture of 200 ml of toluene/l00 ml of dioxane. 5.94 g (58.68 umol) of triethylamine is added and heated for 12 hours to 70C. It is evaporated to the dry state, the residue is taken up in 600 ml of dichloromethane and extracted three times with 300 ml of 5% aqueous potassium carbonate solution each. The organic phase is dried on magnesium sulfate and evaporated to the dry state in a vacuum. The residue S* is chromatographed on silica gel (mobile solvent: ethyl acetate/ethanol 15:1).

Yield: 31.65 g (64% of theory) of a colorless solid Elementary analysis: Cld: C 61.27 H 5.50 N 13.29 Fnd: C 61.15 H 5.61 N 13.10 d) l-(Carboxymethoxyacetyl)-4,7,10-tris{3,5-bis-[4benzyloxycarbonyl-2-oxo-1, 4-diazabutyl]-benzoyl}-l,4 ,7,10tetraazacyclododecane 3.1 g (26.7 mmol) of diglycolic acid anhydride and 5.4 g (53.4 mmol) of triethylamine are added to 30 g (17.8 mmol) of the title compound of Example jc, dissolved in 150 ml of tetrahydrofuran. It is heated for 6 hours to 50 0 C. The solution is evaporated to the dry state in a vacuum, taken up with 250 ml i of dichloromethane and extracted twice with 150 ml of 5% aqueous hydrochloric acid each. The organic phase is dried on magnesium sulfate, evaporated to the dry state in a vacuum, and the residue is chromatographed on silica gel (mobile solvent: dichloromethane/methanol 20:1).

Yield: 29.83 g (93% of theory) of a colorless solid Elementary analysis: Cld: C 59.99 H 5.37 N 12.44 Fnd: C 59.81 H 5.45 N 12.29 e) Completely protected benzyloxycarbonyl-36mer-polyamine, synthesized from N,N,N',N',N",N"-hexakis(2-aminoethyl)trimesic acid triamide-core and six amine-protected hexaamine-monocarboxylic acids described in Example 8d 1.27 g (1 mmol) of the hexa-benzyloxycarbonylamine described in Example le above is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 60 minutes, the incipient precipitation is completed with diethyl ether, the hexamine-hydrobromide produced is washed with ether, dried in a vacuum and used without further purification in the reaction further described below.

Yield: 0.95 g (quantitative) 13.5 g (7.5 mmol) of the cyclene-carboxylic acid described in Example 8d above, 1.2 g (7.5 mmol) of 1-hydroxybenzotriazole and 2.4 g (7.5 mmol) of 2-(H-benztriazl--yl)- ,3 and 2.4 g (7.5 mmol) of 2-(iH-benzotriazol-l-yl)-1,l,3,3- 94 tetramethyluronium tetrafluoroborate (TBTU; Peboc Limited, UK) are dissolved in DMF and stirred for 15 minutes. This solution is then mixed with 5.16 ml (30 mmol) of N-ethyldiisopropylamine and mixed with 0.95 g (1 mmol) of the above-described hexaaminehydrobromide and stirred overnight at room temperature. After the reaction is completed, it is concentrated by evaporation in a vacuum, and the residue is chromatographed on silica gel with dichloromethane/methanol Yield: 8.75 g (81% of theory) of a colorless powder Elementary analysis: Cld: C 64.34 H 5.62 N 13.61 .o Fnd: C 64.22 H 5.86 N 13.51 MALDI-TOF mass spectrum: molar peak at 10,832 (M+Na*) based on the polyamine described in Example 8e 2.16 g (0.2 mmol) of the 3 6mer-benzyloxycarbonylamine described in Example e is dissolved in glacial acetic acid and mixed with 33% hydrogen bromide in glacial acetic acid while being stirred. After 5 hours, the incipient precipitation is completed with diethyl ether, the 36mer-amine-hydrobromide produced is washed with ether and dried in a vacuum and reacted without further purification.

Yield: 1.8 g (quantitative) sei ;ry> f-#~M 1.8 g of the above-described 36mer amine-hydrobromide in 100 ml of DMF is mixed with 17.4 g (20 mmol) of the p-nitrophenylactivated ester described in Example 2e. Within one hour, a solution of 5.05 g (50 mmol) of triethylamine in 20 ml of DMF is then slowly added in drops, so that the precipitate forming at the beginning can again dissolve. It is stirred overnight at 0 C, then the solution is concentrated by evaporation in a vacuum, the residue is dissolved at 0 C in trifluoroacetic acid and stirred overnight at room temperature. It is concentrated by evaporation in a vacuum, the residue is stirred with diethyl ether, the precipitate is suctioned off and.dried in a vacuum.

The acidic crude product is ultimately dissolved in water, set at ge pH 7 with dilute sodium hydroxide solution and ultrafiltered with an AMICON R YM-3 membrane. The retentate is freeze-dried.

Yield: 4.6 g (84% of theory)

H

2 0 content (Karl-Fischer): Elementary analysis (relative to anhydrous substance): Cld: C 47.18 H 5.66 N 16.08 Na 10.00 Fnd: C 47.31 H 5.52 N 16.30 Na 9.57 g) 36mer-Gd complex of the ligand described in the example above 2.74 g (0.1 mmol) of the sodium salt of the complexing agent acid described in Example 8f above is acidified in water with ml of glacial acetic acid, mixed with 725 mg (2 mmol) of Gd 2

O

3 and complexed for 2 hours at 80°C. After cooling, the solution

I

l -l v fi- ;i I- I iii;n;i is filtered, the filtrate is ultrafiltered with YM3 (AMCoN(R)), and the retentate is set -at minimum conductivity by alternately adding cation exchanger IR 120 (W1 f orm) and anion exchanger IRA -410 (OH' form). Exchanger is filtered out, and the filtrate is freeze-dried.

Yield: 2.27 g (74% of theory) of a colorless, flocculent powderi 11.0 content (KtarlFicer).: 8.6% Gd determination* 18.2% NALDI-TOF mass.;spectrum:, molar peak at 27,992 Da (Cld: 28,001 Da) *Elementary analysis ,(relative-to anhydrous substance): Cld: C 41.82 H 5.0.2 -Gd 20.22 N 14.26 '*-PotFnd: C.41.99 H 4.96. Gd 19.87 -N 14.40 .~"INNW~I Ir~I~tt Example for an In Vivo Comparison with an Extracellular Contrast Medium The suitability of the compound described in Example fl as a blood-pool agent is shown in the following test.

As test animals, three male (Schering-SPF) rats that are 200-250 g in weight are used. 0.2 ml (respectively 25 mmol/L) of the following contrast medium solution per animal is administered intravenously: mixture of 1 part each of the compound of 11, named compound 1 below, and the dysprosium complex of 3,6,9triaza-3,6,9-tris(carboxymethyl)-undecanedioic acid (Dy-DTPA), eoooo.

S

named compound 2 below. Blood samples are taken with a catheter 0 in the common carotid artery at the following times: 1, 3, C S 0" 10, 15, 20, 30, 45, 60, 90, 120 minutes p.i. In the blood 0" samples obtained, the concentrations of gadolinium (Gd) and dysprosium (Dy) are measured with the aid of atomic emission 0@S spectrometry (ICP-AES) in each case in a parallel manner. The o. portion of the injected contrast medium of compound 1 (Gd) and compound 2 (Dy, comparison substance), remaining in the blood space, can be compared in the same animals by the different marking. The a- and b-half-lives, the volume of distribution as well as the total clearance can be calculated from the blood concentrations with the aid of special software (Topfit program).

These data thus supply indications on compounds remaining in the intravascular space, the ratios of distribution in the organism and the excretion.

S

Results: Mainly earlier on, considerably higher blood concentrations of compound 1 compared to the extracellular contrast medium (compound 2) are obtained (see Figure 1).

The considerably higher blood concentrations of compound 1 earlier on (compared to compound 2) point to a considerably lower volume of distribution (see also Vd ss), compound 1 is not dispersed as compound 2 in the intravascular space (vessels) and in the extracellular space, but for the most part only in the intravascular space. Later on, the blood level drops quickly, however, and the excretion time or B-half-life of compound 1 is i considerably shorter than in the case of other blood-pool-agents.

The total blood clearance of compound 1 is only somewhat lower compared to compound 2, which can indicate a similarly good renal excretion.

Thus, the compound described in Example 11 has the o requirements of a blood-pool agent: efficient excretion from the blood (through the kidneys), but a considerably lower volume of distribution than an extracellular contrast medium.

U- x- 1L Fig. 1 Measured blood concentrations of Gd (compound 1) and Dy (compound 2) in rats (n 3) [Key:] Verbindung Compound [pmol/L] 1500 I o-Verbindung 1 (Gd) Verbindung 2 (Dy) 1000 0 20 40 t [min p.i.] Compound 1 (Gd) Compound 2 (Dy) Unit a- th 3.0 0.6 1.5 0.5 min 8- th 36.5 18.2 19.2 2.5 min Vd as 0.18 0.07 0.41 0.04 L/kg Total Clearance 13.6 1.5 16.8 0.9 ml/min*kg ;vY

Claims (9)

1. A compound of the formula I'A R 1 OOC-R 2 HC R 3 N-CH 2 -CH 2 -N I I CH 2 CH 2 (I'A) 1 I CH 2 CH 2 I I S. N-CH--CH2-N S' CHR 2 -COOR 1 CHR 2 -COOR' wherein R, independently of one another, stand for a hydrogen atom, a metal ion equivalent of S. atomic numbers 20-29, 39, 42-44 or 57-83 or an acid protective group, R 2 stands for a hydrogen atom, a methyl or an ethyl radical, which optionally is substituted with 1-2 hydroxy or 1 carboxy group(s), R 3 stands for a SR 4 R -CH-CO-N-U 7 -r group, R 4 stands for a hydrogen atom, U 7 stands for a straight-chain, branched, saturated or unsaturated Ci-C 20 alkylene group optionally containing 1-5 imino, 1-3 phenylene, 1-3 phenylenoxy, 1-3 phenylenimino, 1-5 amide, 1-2 hydrazide, 1-5 carbonyl, 1-5 ethylenoxy, 1 urea, 1 thiourea, 1-2 carboxyalkylimino, 1-2 ester groups; 1-10 oxygen, 1-5 sulfur and/or nitrogen atom(s); and optionally substituted by 1-5 hydroxy, 1-2 mercapto, oxo, 1-5 thioxo, 1-3 carboxy, 1-5 carboxyalkyl, 1-5 ester and/or 1-3 amino group(s); whereby the phenylene groups that are optionally contained can be substituted by 1-2 carboxy, 1-2 sulfo or 1-2 hydroxy groups, Z T' stands for a C*O, -COOH, -N=C=O or -N=C=S group, and a, P:\WPDOCHjwSpecsUS 6OS1419cbh-.do-17101/01 -101- C*O stands for an activated carboxyl group.

2. A compound according to claim 1, wherein U 7 is an alkylene group containing at least one -CH 2 NHCO-, -NHCOCH 2 -NHCOCH 2 OC 6 H 4 -N(CH 2 CO 2 -NCOCH 2 C 6 H 4 -NHCSNHC 6 H 4 -CH 2 0C 6 H 4 or -CH 2 CH 2 O- and/or substituted by at least one -COOH or -CH 2 COOH group.

3. A compound according to claim 1, wherein U 7 stands for a -CH 2 CH 2 -CH 2 CH 2 CH 2 -C 6 H 4 -C 6 H 1 0 -CH 2 C 6 H 5 -CH 2 NHCOCH2CH(CH 2 CO2H)-C6H4, -CH 2 NHCOCH20CH 2 -CH 2 NHCOCH 2 C 6 H 4 -CHNHCSNH-C6H 4 -CH(CH 2 COOH)CHz-, -CH 2 OC 6 H 4 -N(CH 2 COOH)CH2-, -CHNHCOCH 2 O(CH 2 CH 2 )4-C6H4-, -CH 2 O-C 6 H 4 -CH 2 CH 2 -O-CH 2 CH 2 -CH 2 CH 2 CH 2 CH 2 -O-CH2CH2, S0 3 H C0 2 H group.

4. A compound according to claim 1, wherein U7 is -CH 2 A compound according to claim 1, wherein R' is a metal ion equivalent of a paramagnetic element.

P:WPDOCS\HjwSpeclUS 6057419dlaim.doc-17/OIm -102-

6. A compound according to claim 5, wherein R' is a metal ion equivalent of gadolinium (III), terbium (III), dysprosium (III), holmium (III), erbium (III), manganese (III) or iron (III).

7. A compound according to claim 1, wherein R' is a metal ion equivalent of the element lanthanum (III) or an element from the lanthanide series.

8. A compound according to claim 1, wherein the activated carboxyl group, is selected from the group consisting of an anhydride, p-nitrophenyl ester, N- hydroxysuccinamide ester, pentafluorophenyl ester and acid chloride.

9. A compound according to claim 1, wherein the acid protective group for R' is a methyl, ethyl, propyl, butyl, phenyl, benzyl, diphenylmethyl, triphenylmethyl, bis-(p- nitrophenyl)-methyl or trialkylsilyl group. DATED this 17th day of January 2001 Schering Aktiengesellschaft By its Patent Attorneys DAVIES COLLISON CAVE h( yy 1-