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JPS636079B2 - - Google Patents
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JPS636079B2 - - Google Patents

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Publication number
JPS636079B2
JPS636079B2 JP7454979A JP7454979A JPS636079B2 JP S636079 B2 JPS636079 B2 JP S636079B2 JP 7454979 A JP7454979 A JP 7454979A JP 7454979 A JP7454979 A JP 7454979A JP S636079 B2 JPS636079 B2 JP S636079B2
Authority
JP
Japan
Prior art keywords
phosphorylcholine
general formula
choline
reaction
cdp
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP7454979A
Other languages
Japanese (ja)
Other versions
JPS55167298A (en
Inventor
Takeshi Kawashima
Osamu Maruyama
Sada Kanai
Makoto Yokoyama
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kojin Co Ltd
Original Assignee
Kojin Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kojin Co Ltd filed Critical Kojin Co Ltd
Priority to JP7454979A priority Critical patent/JPS55167298A/en
Publication of JPS55167298A publication Critical patent/JPS55167298A/en
Publication of JPS636079B2 publication Critical patent/JPS636079B2/ja
Granted legal-status Critical Current

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Description

【発明の詳现な説明】 本発明はシチゞンゞリン酞コリン以䞋、
CDP−コリンず略す。を工業的に補造する方法
に関する。
Detailed Description of the Invention The present invention provides choline cytidine diphosphate (hereinafter referred to as
Abbreviated as CDP-choline. ).

CDP−コリンは脳倖傷時の意識障害および機
胜障害の回埩に甚いられおいる重芁な医薬であ
り、その補造方法も各皮知られおいる。䟋えば、
(1)シチゞン−5′−リン酞以䞋、5′−CMPず略
す。ずホスホリルコリンを瞮合せしめる方法。
特公昭35−13024、特公昭46−37594、特公昭46
−18990、等。(2)5′−CMPの掻性化誘導䜓ずホ
スホリルコリンを反応させる方法。特公昭42−
1384、特公昭46−2101、等。(3)ホスホリルコリ
ンの掻性化誘導䜓ず5′−CMPを反応させる方法。
特公昭45−4747、特公昭52−16115、等。(4)シ
チゞン−5′−ゞリン酞゚タノヌルアミンを経由す
る方法。特公昭39−6541、特開昭47−11476、
等。等が知られおいる。しかしながらこれらの
方法は、高䟡な詊薬の䜿甚、反応、操䜜、収率の
いずれか、たたはその二぀以䞊の点で䞍利な点が
あり工業的に必ずしも有利な方法ではない。
CDP-choline is an important drug used for recovery from impaired consciousness and functional impairment caused by brain trauma, and various methods for its production are known. for example,
(1) A method of condensing cytidine-5'-phosphate (hereinafter abbreviated as 5'-CMP) and phosphorylcholine.
(Tokuko Sho 35-13024, Sho 46-37594, Sho 46
−18990, etc. )(2) A method of reacting an activated derivative of 5′-CMP with phosphorylcholine. (Tokuko Showa 42-
1384, Special Publication Showa 46-2101, etc. )(3) A method of reacting an activated derivative of phosphorylcholine with 5'-CMP.
(Special Publication No. 45-4747, No. 52-16115, etc.) (4) Method via cytidine-5'-diphosphate ethanolamine. (Special Publication No. 39-6541, No. 47-11476,
etc. ) etc. are known. However, these methods have disadvantages in the use of expensive reagents, reaction, operation, yield, or both, and are not necessarily industrially advantageous.

本発明者らはかかる埓来法の欠点をなくし安䟡
で、反応、操䜜が簡単で工業的に有利なCDP−
コリンの補造法を確立する目的で鋭意研究した結
果、取扱い易く、安䟡でしかも反応性に豊む新芏
な䞀般匏〔〕 匏䞭2はモルホリノ基、たたは䜎玚ゞア
ルキルアミノ基を瀺す。で衚わされる䞭間䜓
ホスホリルコリンゞアミデヌト類を芋い出した。
埓来ホスホリルコリンのアミド類に぀いおはモノ
眮換アミド類しか知られおいなか぀たが、䟋え
ば特公昭45−27561、特開昭47−38929、西独特蚱
公開2359245これはホスホリルコリン、あるい
はそのハロゲニドの堎合も、正に荷電した分子内
の第四玚アンモニりム型窒玠が、その分子内で塩
を䜜り易く、リン酞残基の個の氎酞基のうちの
個しか゚ステル化やアミド化されない為に合成
が困難であるずされおいた。本発明者らは鋭意研
究の結果、文献未蚘茉のホスホリルコリンのゞア
ミド類を安䟡な工業薬品より容易に補造し、か぀
本化合物ず、5′−CMPずを溶媒の存圚䞋あるい
は非存圚䞋に、たた酞、塩基の存圚䞋あるいは非
存圚䞋に反応せしめるこずによ぀お、埓来法の欠
点をなくし、短時間でしかも奜収率にCDP−コ
リンを埗る方法を芋い出し、本研究を完成するに
至぀た。すなわち本発明によれば、前蚘䞀般匏
〔〕ホスホリルコリンゞアミデヌト類ず5′−
CMPずを反応せしめるこずにより、CDP−コリ
ンが奜収率で埗られる。
The present inventors have solved the drawbacks of such conventional methods, and have developed CDP-CDP, which is inexpensive, easy to react and operate, and is industrially advantageous.
As a result of intensive research aimed at establishing a method for producing choline, we discovered a new general formula that is easy to handle, inexpensive, and highly reactive. (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group.) Intermediate represented by:
Phosphorylcholine diamidates were discovered.
Conventionally, only monosubstituted amides of phosphorylcholine were known (for example, Japanese Patent Publication No. 45-27561, Japanese Patent Publication No. 47-38929, West German Patent Publication No. 2359245). Difficult to synthesize because the positively charged quaternary ammonium nitrogen in the molecule easily forms salts within the molecule, and only one of the two hydroxyl groups in the phosphoric acid residue is esterified or amidated. It was said to be. As a result of intensive research, the present inventors have found that phosphorylcholine diamides, which have not been described in any literature, can be easily produced using inexpensive industrial chemicals, and the present inventors can easily produce diamides of phosphorylcholine, which have not been described in literature, by combining the present compound and 5'-CMP in the presence or absence of a solvent. Furthermore, by conducting the reaction in the presence or absence of acids and bases, we discovered a method to eliminate the drawbacks of conventional methods and obtain CDP-choline in a short period of time and in good yields, leading to the completion of this research. Ivy. That is, according to the present invention, the phosphorylcholine diamidates of the general formula [] and 5'-
By reacting with CMP, CDP-choline can be obtained in good yield.

本発明においお甚いられる出発原料の぀であ
るホスホリルコリンゞアミデヌト類は埌蚘で詳现
に瀺す通り、䟋えばβ−クロロ゚チルホスホリル
ゞアミデヌト類をトリメチルアミンず反応せしめ
るこずにより、容易にか぀奜収率で埗るこずが出
来る。
As shown in detail later, phosphorylcholine diamidates, which are one of the starting materials used in the present invention, can be obtained easily and in good yield by, for example, reacting β-chloroethylphosphoryl diamidates with trimethylamine. You can get it.

本発明に甚いられる溶媒ずしおは、反応を阻害
しない溶媒であれば、䜕でも良く、たた特に無氎
にする必芁はない。望たしくは、ゞメチルホルム
アミド、ゞメチルアセトアミド、等が有利である
が、無溶媒䞋でも実斜されうる。反応枩床ずしお
は、宀枩から溶媒の沞点たで実斜されるが、望た
しくは、80゜〜140℃が有利である。反応時間は30
分から24時間たで実斜されるが、望たしくは、
〜時間が有利である。ホスホリルコリンゞアミ
デヌト類は5′−CMPに察し等モル以䞊䜿甚する
こずができる。
Any solvent may be used in the present invention as long as it does not inhibit the reaction, and there is no particular need to make it anhydrous. Preferably, dimethylformamide, dimethylacetamide, etc. are used, but it can also be carried out without a solvent. The reaction temperature is from room temperature to the boiling point of the solvent, preferably from 80° to 140°C. reaction time is 30
It is carried out from 1 minute to 24 hours, but preferably 1
~4 hours is advantageous. Phosphorylcholine diamidates can be used in an amount equal to or more than 5'-CMP.

反応系に存圚せしめる酞ずしおは、トリクロル
酢酞等の有機酞が奜たしいが、硫酞、塩化氎玠等
の無機酞でも良い。酞の䜿甚量は䜿甚するホスホ
リルコリンゞアミデヌトの0.01からモル量皋床
が奜たしい。
The acid to be present in the reaction system is preferably an organic acid such as trichloroacetic acid, but may also be an inorganic acid such as sulfuric acid or hydrogen chloride. The amount of acid used is preferably about 0.01 to 1 mole of the phosphorylcholine diamidate used.

反応混合物から目的物を単離するには、垞法に
埓぀お行えば良い。䟋えば反応埌、溶媒を留去す
るかたたは䞊柄を傟斜しお陀くか、たたは溶媒を
加えお沈柱させるかしお、埗られた残枣を氎に溶
解し、アニオン亀換暹脂により目的物を吞着せし
め、次いで垌ギ酞氎溶液で溶離させる。溶離した
CDP−コリン区分を集め、濃瞮、也燥しお目的
物のCDP−コリンを埗る。
The target product can be isolated from the reaction mixture by a conventional method. For example, after the reaction, the solvent is distilled off, the supernatant is decanted, or a solvent is added to precipitate, the resulting residue is dissolved in water, and the target product is adsorbed by an anion exchange resin. , followed by elution with dilute aqueous formic acid. eluted
The CDP-choline fraction is collected, concentrated and dried to obtain the target product, CDP-choline.

本発明の特城は非垞に掻性床の高い前蚘䞀般匏
〔〕の化合物をCDP−コリンの合成に利甚する
点にある。即ち䞀般匏〔〕の化合物は5′−
CMPず反応し䞀旊䞋蚘䞀般匏〔〕、 匏䞭2はモルホリノ基、たたは䜎玚ゞア
ルキルアミノ基を瀺す。を反応䞭間䜓ずしお䞎
えるが、反応条件䞋、このものを単離するこずな
く加氎分解を経おほずんど定量的にか぀高玔床に
CDP−コリンを埗る点にある。曎に䞀般匏〔〕
の化合物を利甚するこずにより適圓な溶媒䟋え
ばゞメチルアセトアミド等を遞ぶこずにより、
5′−CMPのトリ−ブチルアミン塩をオルトク
ロロプノヌル溶媒䞭ホスホリルコリンモノアミ
デヌトず反応させる公知䟋特公昭45−4747の
劂く5′−CMPを䞀旊トリ−ブチルアミン塩な
どの有機アミン塩化する必芁もなく5′−CMP自
䜓で反応させるこずが出来る。たた、䞀般匏
〔〕ず5′−CMPの反応の反応時間は先に匕䟋の
特公昭45−4747の䟋瀺の堎合の100℃、18時間に
比べ100℃、時間ずきわめお短かく、か぀反応
埌の操䜜も溶媒を特に留去する必芁なく䞊柄を傟
斜しお陀くこずが出来る等きわめお工業的に優れ
た有利な方法である。
A feature of the present invention is that the compound of the general formula [], which has a very high activity, is utilized for the synthesis of CDP-choline. That is, the compound of general formula [] is 5'-
Once reacted with CMP, the following general formula [], (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group) is provided as a reaction intermediate, but under the reaction conditions, it is hydrolyzed without isolation, almost quantitatively and High purity
The point is to obtain CDP-choline. Furthermore, the general formula []
By selecting an appropriate solvent (e.g. dimethylacetamide, etc.),
5'-CMP is first converted into an organic amine salt such as tri-n-butylamine salt, as in a known example (Japanese Patent Publication No. 45-4747) in which tri-n-butylamine salt of 5'-CMP is reacted with phosphorylcholine monoamidate in an orthochlorophenol solvent. The reaction can be carried out with 5'-CMP itself without the need for further reaction. In addition, the reaction time for the reaction between the general formula [] and 5'-CMP is extremely short at 100°C for 3 hours, compared to 18 hours at 100°C in the case of the example cited in Japanese Patent Publication No. 45-4747. The subsequent operation is also an extremely industrially advantageous method in which the supernatant can be removed by decanting without the need to specifically distill off the solvent.

本発明における䞀般匏〔〕の化合物であるホ
スホリルコリンゞアミデヌト類は以䞋に述べる䞉
方法で補造可胜であり個々の化合物、反応条件等
により適切な方法を遞ぶこずが出来るがこれらの
詳现に぀いお以䞋順を远぀お説明する。
Phosphorylcholine diamidates, which are compounds of the general formula [] in the present invention, can be produced by the three methods described below, and an appropriate method can be selected depending on the individual compound, reaction conditions, etc. Details of these methods are as follows: I will explain later.

補造法(1) 匏䞭、2はモルホリノ基、たたは䜎玚ゞ
アルキルアミノ基を瀺す。で瀺される劂く、ク
ロロ゚チルホスホリルゞアミデヌト類䞀般匏
〔〕を経由する。β−クロロ゚チルホスホリル
ゞクロリド文献䟋、J.Amer.Chem.Soc.、51、
9531929に無氎有機溶媒䞭でモルホリンたた
は䜎玚ゞアルキルアミンず反応させるこずにより
䞀般匏〔〕の化合物を埗る。぀いで䞀般匏
〔〕の化合物から䞀般匏〔〕ぞの化合物の倉
換は、封管䞭トリメチルアミンず反応させるこず
により高収率で埗られる。反応溶媒ずしおは、反
応を阻害しない溶媒なら䜕でも良いが䟋えば、ベ
ンれン等の芳銙族炭化氎玠類、クロロホルム等の
ハロゲン化氎玠類、テトラハむドロフラン等の゚
ヌテル類、アセトン等のケトン類、アセトニトリ
ル等のニトリル類、ゞメチルホルムアミド等のア
ミド類を挙げるこずが出来るが、有利には、アセ
トニトリル等のニトリル類が望たしい。反応枩床
は宀枩から溶媒の沞点の間で実斜されるが、望た
しくは50゜〜100℃の枩床で実斜される。反応時間
は、数時間から数日間で実斜される。反応生成物
は、反応液を濃瞮するこずにより結晶たたはオむ
ルずしお埗られる。
Manufacturing method (1) (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group.) via chloroethylphosphoryl diamidates (general formula []). β-chloroethylphosphoryl dichloride (Reference example, J.Amer.Chem.Soc., 51 ,
953 (1929)) with morpholine or lower dialkylamine in an anhydrous organic solvent to obtain a compound of general formula []. Then, the compound of general formula [] is converted into general formula [] by reacting it with trimethylamine in a sealed tube in a high yield. Any reaction solvent may be used as long as it does not inhibit the reaction, but examples include aromatic hydrocarbons such as benzene, hydrogen halides such as chloroform, ethers such as tetrahydrofuran, ketones such as acetone, and acetonitrile. Mention may be made of nitriles and amides such as dimethylformamide, but advantageously nitriles such as acetonitrile are preferred. The reaction temperature is between room temperature and the boiling point of the solvent, preferably between 50° and 100°C. Reaction times range from several hours to several days. The reaction product is obtained as crystals or oil by concentrating the reaction solution.

本補造法は䞀般匏〔〕の化合物を容易にか぀
安䟡に補造せしめる点においお工業的にすぐれお
いる。
This production method is industrially superior in that it allows the compound of general formula [] to be produced easily and at low cost.

補造法(2) 匏䞭、2はモルホリノ基、および䜎玚ゞ
アルキルアミノ基を瀺す。 コリンクロリドず公知のクロロホスホリルゞア
ミデヌト䞀般匏〔〕文献䟋、J.Chem.
Soc.、1958、1963ずを塩基存圚䞋反応させるこ
ずにより䞀般匏〔〕で衚わされる、ホスホリル
コリンゞアミデヌトクロラむド〔〕が埗られ
る。反応溶媒ずしおは、極性有機溶媒、䟋えば、
ゞメチルホルムアミド、ゞメチルスルホキシド等
を挙げるこずが出来る。塩基ずしおは、氎玠化ナ
トリりム等の無機塩基、・・−ルチゞン、ピ
リゞン等の有機塩基が甚いられる。反応枩床ずし
おは、宀枩から溶媒の沞点の間で実斜されるが、
望たしくは、宀枩から150℃で実斜される。反応
時間は、数時間から数日間実斜されるが、有利に
は、時間前埌が望たしい。反応生成物は、沈柱
物を濟取し、濟液を枛圧濃瞮するこずにより、ホ
スホリルコリンゞアミデヌトクロラむドの結晶た
たはオむルずしお埗られる。
Manufacturing method (2) (In the formula, N(R) 2 represents a morpholino group and a lower dialkylamino group.) Choline chloride and the known chlorophosphoryl diamidate (general formula []) (Reference examples, J.Chem.
Soc., 1958 , 1963) in the presence of a base to obtain phosphorylcholine diamidate chloride [] represented by the general formula []. As the reaction solvent, polar organic solvents such as
Dimethylformamide, dimethylsulfoxide, etc. can be mentioned. As the base, an inorganic base such as sodium hydride, an organic base such as 2,6-lutidine, pyridine, etc. are used. The reaction temperature is between room temperature and the boiling point of the solvent,
Desirably, it is carried out at room temperature to 150°C. The reaction time ranges from several hours to several days, but is preferably around 8 hours. The reaction product is obtained as crystals or oil of phosphorylcholine diamidate chloride by filtering the precipitate and concentrating the filtrate under reduced pressure.

本補造法は䞀般匏〔〕の化合物を収率良く補
造せしめる点においおすぐれた方法である。
This production method is an excellent method in that it allows the compound of general formula [] to be produced with good yield.

補造法(3) 匏䞭、2はモルホリノ基、および䜎玚ゞ
アルキルアミノ基を瀺す。 公知のホスホリルコリンゞクロリデヌト文献
䟋、Compt.Rend.、257、183、1963、特公昭47
−32970ずモルホリン、たたは䜎玚アルキルア
ミンを反応させるこずにより、䞀般匏〔〕で衚
わされるホスホリルコリンゞアミデヌトクロラむ
ドが埗られる。反応溶媒ずしおは、ゞメチルホル
ムアミド、ゞメチルスルホキシド、アセトニトリ
ル等の極性溶媒が甚いられるが、無溶媒でも実斜
される。反応枩床ずしおは、氷点䞋から溶媒の沞
点の間で実斜されるが、有利には、−℃から宀
枩の間が望たしい。反応時間ずしおは、数時間か
ら数日間実斜されるが、有利には、数時間が望た
しい。反応生成物は、沈柱を濟取し、濟液を枛圧
濃瞮するこずにより、ホスホリルコリンゞアミデ
ヌトクロラむドの結晶たたは、オむルずしお埗ら
れる。本補造は䞀般匏〔〕の化合物を短時間に
か぀容易に補造せしめる点ですぐれおいる。
Manufacturing method (3) (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group.) Known phosphorylcholine dichloridate (Literature example, Compt. Rend., 257 , 183, (1963), Japanese Patent Publication No. 47
-32970) with morpholine or lower alkylamine, phosphorylcholinediamidate chloride represented by the general formula [] is obtained. As the reaction solvent, polar solvents such as dimethylformamide, dimethylsulfoxide, acetonitrile, etc. are used, but the reaction can also be carried out without a solvent. The reaction temperature is carried out between below freezing and the boiling point of the solvent, preferably between -5°C and room temperature. The reaction time ranges from several hours to several days, and advantageously several hours. The reaction product is obtained as crystals or oil of phosphorylcholine diamidate chloride by filtering the precipitate and concentrating the filtrate under reduced pressure. This production is excellent in that it allows the compound of the general formula [] to be produced easily and in a short time.

以䞋に本発明の実斜䟋を䞊げ詳现に説明する
が、これらは本発明を限定するものではない。
Examples of the present invention will be described in detail below, but the present invention is not limited to these examples.

実斜䟋  ホスホリルコリンゞモルホリデヌトクロラむド
䞀般匏〔〕、2モルホリノ基1.2ず
5′−CMP1をゞメチルアセトアミド4.5mlに懞濁
し100℃、時間撹拌䞋反応せしめる。反応埌䞊
柄のゞメチルアセトアミドを傟斜しお陀き、残枣
を氎に溶解し、アンモニア氎でPH9.5に調敎し、
ダむアむオンSA11Bギ酞型120mlに吞着せし
め、0.01〜0.03Mギ酞により溶離する。CDP−コ
リンのフラクシペンを集めお濃瞮し、也燥するこ
ずによりCDP−コリン1.44を埗た。なお本化合
物は、ペヌパヌクロマトグラフむヌ゚タノヌ
ル、0.5M−酢酞アンモン高圧濟玙電気
泳動0.2M−リン酞バツフアヌPH7.4、1500V、
時間、栞磁気共鳎吞収スペクトル重氎䞭、
赀倖線吞収スペクトル臭化カリりムデむスク、
玫倖線吞収スペクトルPH11、PH7.0、PH1.5で
暙品のCDP−コリンず完党に䞀臎した。
Example 1 1.2 g of phosphorylcholine dimorpholito chloride (general formula [ ], N(R) 2 = morpholino group)
1 g of 5'-CMP was suspended in 4.5 ml of dimethylacetamide and reacted at 100°C for 3 hours with stirring. After the reaction, the supernatant dimethylacetamide was decanted, the residue was dissolved in water, and the pH was adjusted to 9.5 with aqueous ammonia.
Adsorb to 120 ml of Diaion SA11B (formic acid type) and elute with 0.01-0.03M formic acid. CDP-choline fractions were collected, concentrated, and dried to obtain 1.44 g of CDP-choline. This compound was analyzed by paper chromatography (ethanol, 0.5M ammonium acetate 5:2), high pressure filter paper electrophoresis (0.2M phosphate buffer PH7.4, 1500V,
2 hours), nuclear magnetic resonance absorption spectrum (in heavy water),
Infrared absorption spectrum (potassium bromide disk),
The ultraviolet absorption spectrum (PH11, PH7.0, PH1.5) completely matched that of standard CDP-choline.

実斜䟋  ホスホリルコリンゞモルホリデヌトクロラむド
1.2ず5′−CMP1.0を混和し、100℃で撹拌䞋
時間加熱反応せしめる。反応埌反応混合物を氎
に溶解し、実斜䟋ず同様にむオン亀換暹脂によ
る粟補凊理を行い、CDP−コリン分画を集めお
濃瞮し、也燥するこずにより、CDP−コリンの
玔品1.28を埗た。こうしお埗られたCDP−コリ
ンは実斜䟋ず同様に、暙品のCDP−コリンず
比范同定したずころ、完党に䞀臎した。
Example 2 Phosphorylcholine dimolholitochloride
1.2 g and 1.0 g of 5'-CMP were mixed and reacted by heating at 100°C for 4 hours with stirring. After the reaction, the reaction mixture was dissolved in water, purified using an ion exchange resin in the same manner as in Example 1, and the CDP-choline fraction was collected, concentrated, and dried to obtain 1.28 g of pure CDP-choline. Obtained. The thus obtained CDP-choline was compared and identified with the standard CDP-choline in the same manner as in Example 1, and it was found to be completely identical.

実斜䟋  ホスホリルコリンゞモルホリデヌトクロラむド
1.2ず5′−CMP1.0をゞメチルアセトアミド4.5
mlに懞濁し、100℃、時間撹拌䞋反応せしめる。
反応埌䞊柄のゞメチルアセトアミドを傟斜しお陀
き、残枣を氎に溶解し、実斜䟋ず同様にむオン
亀換暹脂による粟補凊理を行い、CDP−コリン
分画を集めお濃瞮し、也燥するこずにより、
CDP−コリンの玔品1.38を埗た。こうしお埗ら
れたCDP−コリンは実斜䟋ず同様に、暙品の
CDP−コリンず比范同定したずころ、完党に䞀
臎した。
Example 3 Phosphorylcholine dimorpholitochloride
1.2g and 1.0g of 5′-CMP with 4.5g of dimethylacetamide
ml and reacted at 100°C for 3 hours with stirring.
After the reaction, the supernatant dimethylacetamide was decanted, the residue was dissolved in water, and purified using an ion exchange resin in the same manner as in Example 1. The CDP-choline fraction was collected, concentrated, and dried. ,
1.38 g of pure CDP-choline was obtained. The thus obtained CDP-choline was prepared in the same way as in Example 1.
When compared and identified with CDP-choline, they were completely identical.

実斜䟋  ホスホリルコリン−・N′−ゞ゚チルゞアミ
デヌトクロラむド䞀般匏〔〕、゚チル
1.98ず5′−CMP0.96をゞメチルアセトアミド
mlに加え、120℃、時間撹拌䞋反応せしめる。
反応埌、実斜䟋ず同様に凊理しお、CDP−コ
リン0.88を埗た。こうしお埗られたCDP−コリ
ンは実斜䟋ず同様に、暙品のCDP−コリンず
比范同定したずころ、完党に䞀臎した。
Example 4 Phosphorylcholine-N・N'-diethyldiamidate chloride (general formula [], R=ethyl)
1.98 g and 0.96 g of 5'-CMP were added to 3 ml of dimethylacetamide and reacted at 120°C for 3 hours with stirring.
After the reaction, the same treatment as in Example 1 was carried out to obtain 0.88 g of CDP-choline. The thus obtained CDP-choline was compared and identified with the standard CDP-choline in the same manner as in Example 1, and it was found to be completely identical.

実斜䟋  β−クロロ゚チルホスホリルゞクロリド10に
ベンれン20mlを加え、氷冷䞋撹拌しながらモルホ
リン17.7をベンれン60mlに溶かした溶液を埐々
に滎䞋する。滎䞋終了埌宀枩で時間撹拌し、析
出したモルホリンの塩酞塩を濟取する。濟液を濃
瞮也固し10℃以䞋で攟眮するず結晶が析出する。
゚ヌテルで結晶を掗滌し也燥するず、融点53゜〜
58℃のβ−クロロ゚チルホスホリルゞモルホリデ
ヌト䞀般匏〔〕、2モルホリノ基の
癜色結晶13.1が埗られた。
Example 5 20 ml of benzene is added to 10 g of β-chloroethylphosphoryl dichloride, and a solution of 17.7 g of morpholine dissolved in 60 ml of benzene is gradually added dropwise while stirring under ice cooling. After the addition was completed, the mixture was stirred at room temperature for 1 hour, and the precipitated morpholine hydrochloride was collected by filtration. If the filtrate is concentrated to dryness and left at 10°C or lower, crystals will precipitate.
When the crystals are washed with ether and dried, the melting point is 53° ~
13.1 g of white crystals of β-chloroethylphosphoryl dimorpholinate (general formula [], N(R) 2 =morpholino group) at 58° C. were obtained.

元玠分析C10H20ClN2O4Pずしお 理論倀 40.21、6.75、9.37 分析倀 40.14、6.83、9.38 次にこのβ−クロロ゚チルホスホリルゞモルホ
リデヌトに、トリメチルアミンの30アセト
ニトリル溶液20を加え、封管䞭70℃で48時間反
応させる。反応埌析出物を濟取し、濟液を濃瞮
し、少量のゞオキサンを加え10℃以䞋で攟眮する
ず結晶化し、融点64゜〜70℃のホスホリルコリン
ゞモルホリデヌトクロラむド䞀般匏〔〕
2モルホリノ基の癜色結晶5.4が埗られ
た。
Elemental analysis (as C 10 H 20 ClN 2 O 4 P) Theoretical value C: 40.21%, H: 6.75%, N: 9.37% Analytical value C: 40.14%, H: 6.83%, N: 9.38% Next, this β - Add 20 g of a 30% acetonitrile solution of trimethylamine to 5 g of chloroethylphosphoryl dimorpholidate and react in a sealed tube at 70° C. for 48 hours. After the reaction, the precipitate is collected by filtration, the filtrate is concentrated, a small amount of dioxane is added, and when it is left to stand at below 10°C, it crystallizes to form phosphorylcholine dimorpholidite chloride (general formula []N
5.4 g of white crystals of (R) 2 =morpholino group) were obtained.

元玠分析C13H29ClN3O4P・H2Oずしお 理論倀41.73、8.36、11.22 分析倀41.85、8.41、11.39 埗られたホスホリルコリンゞモルホリデヌトク
ロラむドを甚い実斜䟋〜のずおり実斜し同じ
くシチゞンゞリン酞コリンを埗た。
Elemental analysis (as C 13 H 29 ClN 3 O 4 P・H 2 O) Theoretical value C: 41.73%, H: 8.36%, N: 11.22% Analytical value C: 41.85%, H: 8.41%, N: 11.39% Using the obtained phosphorylcholine dimorpholithochloride, the same procedure as in Examples 1 to 3 was carried out to obtain choline cytidine diphosphate.

実斜䟋  β−クロロ゚チルホスホロゞクロラむド10に
ベンれン20mlを加え、氷冷䞋撹拌しながら、ゞ゚
チルアミン15.6をベンれン60mlに溶かした溶液
を滎䞋する。滎䞋終了埌宀枩で時間撹拌し、析
出した沈柱を濟取し、濟液を濃緒する。残枣を枛
圧蒞留するこずにより、沞点108℃mmHgの
無色オむル状のβ−クロロ゚チルホスホロ−・
N′−ゞ゚チルゞアミデヌト䞀般匏〔〕
゚チル9.6が埗られた。
Example 6 20 ml of benzene is added to 10 g of β-chloroethylphosphorodichloride, and a solution of 15.6 g of diethylamine dissolved in 60 ml of benzene is added dropwise while stirring under ice cooling. After the addition was completed, the mixture was stirred at room temperature for 1 hour, the precipitate was collected by filtration, and the filtrate was concentrated. By distilling the residue under reduced pressure, β-chloroethylphosphoro-N.
N'-diethyldiamidate (general formula []R=
ethyl) was obtained.

次にこのβ−クロロ゚チルホスホロ−・
N′−ゞ゚チルゞアミデヌトに、トリメチル
アミンの30アセトニトリル溶液20を加え、封
管䞭70℃にお48時間反応せしめる。反応埌、反応
液を濃瞮し、ゞオキサンを加え、䞍溶物を濟取す
る。濟液を濃瞮也固するず、ホスホリルコリン−
・N′−ゞ゚チルゞアミデヌトクロラむド䞀
般匏〔〕゚チルが3.65埗られた。この
ものはペヌパヌクロマトグラフむヌでモノスポツ
トであり゚タノヌル0.5M−酢酞アンモン、
10、HI詊薬で怜出、、ガス、シリカゲル薄
局クロマトグラフむヌでもモノスポツトであ぀た
クロロホルムメタノヌル、、HI詊薬、
ペり玠で怜出、。栞磁気共鳎吞収スペクトル、
ÎŽ1.1712H、、Hz、Ύ3.18H、、、
ÎŽ3.279H、、Ύ3.722H、、Ύ4.352H、
、〔溶媒メタノヌル−d4、内郚暙準TMS、
Varian −60〕 埗られたホスホリルコリン−・N′−ゞ゚チ
ルゞアミデヌトクロラむドを甚い実斜䟋のずお
り実斜し同じくシチゞンゞリン酞コリンを埗た。
Next, this β-chloroethylphosphoro-N・
20 g of a 30% acetonitrile solution of trimethylamine was added to 5 g of N'-diethyldiamidate, and the mixture was allowed to react in a sealed tube at 70° C. for 48 hours. After the reaction, the reaction solution is concentrated, dioxane is added, and insoluble matter is filtered off. When the filtrate is concentrated to dryness, phosphorylcholine-
3.65 g of N.N'-diethyldiamidate chloride (general formula []R=ethyl) was obtained. This is a paper chromatography monospot (ethanol: 0.5M - ammonium acetate,
10:1, detected with HI reagent), gas, and silica gel thin layer chromatography (chloroform:methanol, 1:2, HI reagent,
Detected with iodine). nuclear magnetic resonance absorption spectrum,
ÎŽ1.17 (12H, t, J=7Hz), ÎŽ3.1 (8H, m,),
ÎŽ3.27 (9H, s), ÎŽ3.72 (2H, m), ÎŽ4.35 (2H,
m), [solvent methanol- d4 , internal standard TMS,
Varian T-60] Using the obtained phosphorylcholine-N·N'-diethyldiamidate chloride, the same procedure as in Example 4 was carried out to obtain choline cytidine diphosphate.

実斜䟋  コリンクロリド1.4ずクロロホスホリルゞモ
ルホリデヌト2.55をゞメチルスルホキシドml
に混和し、撹拌しながら氎玠化ナトリりム0.24
を加え、宀枩で時間撹拌䞋反応させる。反応埌
析出した少量の沈柱を濟取し、濟液を枛圧䞋濃瞮
也固する。残枣に少量のアセトニトリルを加え、
濟過し、濟液を濃瞮し、10℃以䞋で攟眮するず、
癜色結晶のホスホリルコリンゞモルホリデヌトク
ロラむド䞀般匏〔〕2モルホリノ基
が2.05埗られた。このものは実斜䟋で埗られ
た結晶ず融点、ペヌパヌクロマトグラフむヌ゚
タノヌル0.5M−酢酞アンモン、10、HI詊
薬で怜出、で完党に䞀臎した。
Example 7 1.4 g of choline chloride and 2.55 g of chlorophosphoryl dimorpholidate were mixed with 5 ml of dimethyl sulfoxide.
0.24 g of sodium hydride while stirring.
was added and reacted at room temperature for 8 hours with stirring. After the reaction, a small amount of precipitate is collected by filtration, and the filtrate is concentrated to dryness under reduced pressure. Add a small amount of acetonitrile to the residue,
Filter, concentrate the filtrate, and leave it at below 10°C.
White crystalline phosphorylcholine dimorpholitochloride (general formula []N(R) 2 = morpholino group)
2.05g of was obtained. This product completely matched the crystals obtained in Example 5 in melting point and paper chromatography (ethanol:0.5M ammonium acetate, 10:1, detected with HI reagent).

埗られたホスホリルコリンゞモルホリデヌトク
ロラむドを甚い実斜䟋〜のずおり実斜し同じ
くシチゞンゞリン酞コリンを埗た。
Using the obtained phosphorylcholine dimorpholithochloride, the same procedure as in Examples 1 to 3 was carried out to obtain choline cytidine diphosphate.

実斜䟋  ホスホリルコリンゞクロリデヌトをアセト
ニトリルmlに加え、撹拌䞋、冷华しながらモル
ホリン1.36を滎䞋する。滎䞋終了埌宀枩で時
間撹拌し、ベンれン10mlを加え、宀枩で曎に30分
間撹拌し、析出した癜色結晶を濟取する。濟液を
濃瞮也固し、残枣に少量のアセトニトリルを加え
濟過し、濟液を10℃䞊䞋で攟眮するず、癜色結晶
のホスホリルコリンゞモルホリデヌトクロラむド
0.56が埗られた。この結晶は実斜䟋で埗られ
た結晶ず融点、ペヌパヌクロマトグラフむヌ、栞
磁気共鳎吞収スペクトルで完党に䞀臎した。
Example 8 1 g of phosphorylcholine dichloridate is added to 4 ml of acetonitrile, and 1.36 g of morpholine is added dropwise while stirring and cooling. After the addition was completed, the mixture was stirred at room temperature for 3 hours, 10 ml of benzene was added, and the mixture was further stirred at room temperature for 30 minutes, and the precipitated white crystals were collected by filtration. The filtrate is concentrated to dryness, a small amount of acetonitrile is added to the residue, it is filtered, and the filtrate is left at 10°C or lower to produce white crystals of phosphorylcholine dimorpholitochloride.
0.56g was obtained. This crystal completely matched the crystal obtained in Example 5 in melting point, paper chromatography, and nuclear magnetic resonance absorption spectrum.

埗られたホスホリルコリンゞモルホリデヌトク
ロラむドを甚い実斜䟋〜のずおり実斜し同じ
くシチゞンゞリン酞コリンを埗た。
Using the obtained phosphorylcholine dimorpholithochloride, the same procedure as in Examples 1 to 3 was carried out to obtain choline cytidine diphosphate.

Claims (1)

【特蚱請求の範囲】  䞀般匏〔〕 匏䞭2はモルホリノ基、たたは䜎玚ゞア
ルキルアミノ基を瀺す。で衚わされるホスホリ
ルコリンゞアミデヌト類ずシチゞン−5′−モノリ
ン酞を反応せしめるこずを特城ずするシチゞンゞ
リン酞コリンの補造方法。  䞀般匏〔〕 匏䞭2はモルホリノ基、たたは䜎玚ゞア
ルキルアミノ基を瀺す。で衚わされるβ−クロ
ロ゚チルホスホリルゞアミデヌトをトリメチルア
ミンず反応させ䞀般匏〔〕で衚わされるホスホ
リルコリンゞアミデヌト類ずし、぀いでシチゞン
−5′−モノリン酞ず反応せしめるこずを特城ずす
るシチゞンゞリン酞コリンの補造方法。  䞀般匏〔〕 匏䞭2はモルホリノ基、たたは䜎玚ゞア
ルキルアミノ基を瀺す。で衚わされるクロロホ
スホリルゞアミデヌト類ずコリンクロリドを反応
させ䞀般匏〔〕で衚わされるホスホリルコリン
ゞアミデヌト類ずし、぀いでシチゞン−5′−モノ
リン酞ず反応せしめるこずを特城ずするシチゞン
ゞリン酞コリンの補造方法。  ホスホリルコリンゞクロリデヌトずモルホリ
ンたたは䜎玚ゞアルキルアミンを反応させ䞀般匏
〔〕で衚わされるホスホリルコリンゞアミデヌ
ト類ずし、぀いでシチゞン−5′−モノリン酞ず反
応せしめるこずを特城ずするシチゞンゞリン酞コ
リンの補造方法。
[Claims] 1. General formula [] (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group.) Production of choline cytidine diphosphate, which is characterized by reacting a phosphorylcholine diamidate represented by the formula with cytidine-5'-monophosphoric acid. Method. 2 General formula [] (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group) is reacted with trimethylamine to obtain phosphorylcholine diamidates represented by the general formula []. , and then reacting with cytidine-5'-monophosphoric acid. 3 General formula [] (In the formula, N(R) 2 represents a morpholino group or a lower dialkylamino group) is reacted with choline chloride to obtain phosphorylcholine diamidates represented by the general formula [ ], A method for producing choline cytidine diphosphate, which comprises then reacting it with cytidine-5'-monophosphoric acid. 4. A method for producing choline cytidine diphosphate, which comprises reacting phosphorylcholine dichloridate with morpholine or lower dialkylamine to obtain phosphorylcholine diamidates represented by the general formula [], and then reacting with cytidine-5'-monophosphoric acid. .
JP7454979A 1979-06-15 1979-06-15 Preparation of cytidine diphosphate choline Granted JPS55167298A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7454979A JPS55167298A (en) 1979-06-15 1979-06-15 Preparation of cytidine diphosphate choline

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7454979A JPS55167298A (en) 1979-06-15 1979-06-15 Preparation of cytidine diphosphate choline

Publications (2)

Publication Number Publication Date
JPS55167298A JPS55167298A (en) 1980-12-26
JPS636079B2 true JPS636079B2 (en) 1988-02-08

Family

ID=13550434

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7454979A Granted JPS55167298A (en) 1979-06-15 1979-06-15 Preparation of cytidine diphosphate choline

Country Status (1)

Country Link
JP (1) JPS55167298A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0282215U (en) * 1988-12-16 1990-06-26

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0282215U (en) * 1988-12-16 1990-06-26

Also Published As

Publication number Publication date
JPS55167298A (en) 1980-12-26

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