JPH0791274B2 - Benzimidazole derivative pharmaceutical composition - Google Patents

Description

FIELD OF THE INVENTION The present invention relates to novel benzimidazole derivative pharmaceutical compositions.

BACKGROUND OF THE INVENTION The present inventors have previously described the following general formula (I): (In the formula, R ¹ represents a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group, a phenyl group or an aralkyl group, and R ² represents a hydrogen atom or a lower alkyl group, or R ¹ and R 2 ² together form a ring with an adjacent nitrogen atom, and R ³ and R ⁴ are each independently a hydrogen atom, a halogen atom, a trifluoromethyl group, a lower alkyl group, a lower alkoxy group, a lower alkoxycarbonyl group or It was found that the novel benzimidazole derivative represented by (showing an amino group) has an excellent gastric acid secretion inhibitory action and is therefore effective as an anti-ulcer agent. A patent application has already been filed for this compound, the synthesis method and the use thereof (Japanese Patent Laid-Open No. Sho 61-61).
-60660, Japanese Patent Application Nos. 60-61194 and 60-61195).

As a result of further intensive research, the present inventors have found that the benzimidazole derivative represented by the general formula (I) has not only a gastric acid secretion inhibitory action but also an excellent cytoprotective action, and therefore, as a gastrointestinal cytoprotective agent. Have also found useful. A patent application has already been filed for the invention of this gastrointestinal cytoprotective agent (Japanese Patent Application No. 60-178951).

Furthermore, the present inventors found that the storage stability of the benzimidazole derivative was not sufficient at the stage of studying the practical use of the drug containing the above-mentioned benzimidazole derivative as an active ingredient, and the improvement of the storage stability was confirmed. Considered as the purpose. As a result, they have found that the storage stability is improved by miniaturizing the benzimidazole derivative. A patent application has already been filed for this invention (Japanese Patent Application No. 61-38286).

[Object of the Invention] An object of the present invention is to provide a novel benzimidazole derivative drug composition.

Another object of the present invention is to provide a benzimidazole derivative drug composition having improved storage stability.

[Structure of the Invention] The present invention has the following general formula (I): (In the formula, R ¹ represents a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group, a phenyl group or an aralkyl group, and R ² represents a hydrogen atom or a lower alkyl group, or R ¹ and R 2 ² together form a ring with an adjacent nitrogen atom, and R ³ and R ⁴ are each independently a hydrogen atom, a halogen atom, a trifluoromethyl group, a lower alkyl group, a lower alkoxy group, a lower alkoxycarbonyl group or A stabilized benzimidazole derivative pharmaceutical composition comprising a benzimidazole derivative having a physiological activity represented by (showing an amino group) and 5% by weight or more of a basic organic substance with respect to the benzimidazole derivative. It is in.

The benzimidazole derivative of the general formula (I) of the present invention is already known as described above, and can be obtained, for example, by the production method described in the above-mentioned publication.

Examples of representative compounds represented by the general formula (I) include the following compounds.

Compound 1: 2- (2-Dimethylaminobenzylsulfinyl) benzimidazole Compound 2: 2- (2-Diethylaminobenzylsulfinyl) benzimidazole Compound 3: 2- (2-Aminobenzylsulfinyl) benzimidazole Compound 4: 2- (2 -Methylaminobenzylsulfinyl) benzimidazole compound 5: 2- (2-dimethylaminobenzylsulfinyl) -5-methoxybenzimidazole compound 6: 2- (2-dimethylaminobenzylsulfinyl) -4-methylbenzimidazole compound 7: 2 -(2-Dimethylamino-6-methylbenzylsulfinyl) benzimidazole compound 8: 2- (2-Dimethylaminobenzylsulfinyl) -5-methoxycarbonylbenzimidazole compound 9: 2- (2-dimethylaminobenzylsulfinyl) ) -5-Methylbenzimidazole compound 10: 5-chloro-2- (2-dimethylaminobenzylsulfinyl) benzimidazole compound 11: 5-amino-2- (2-dimethylaminobenzylsulfinyl) benzimidazole compound 12: 2- (2-Dimethylamino-5-methoxybenzylsulfinyl) benzimidazole Compound 13: 2- (2-dimethylamino-5-methylbenzylsulfinyl) benzimidazole Compound 14: 2- (2-piperidinobenzylsulfinyl)
Benzimidazole compound 15: 2- [2- (N-cyclohexyl-N-methylamino) benzylsulfinyl] benzimidazole compound 16: 2- [2- (N-benzyl-N-methylamino) benzylsulfinyl] benzimidazole In the benzimidazole derivative used in, it is preferable that R ¹ in the general formula (I) is an alkyl group having 1 to 8 carbon atoms. R ² is preferably a lower alkyl group. R ³ is preferably a hydrogen atom or a lower alkoxy group, and R ⁴ is preferably a hydrogen atom or a lower alkyl group. Examples of the lower alkyl group and the lower alkoxy group include alkyl groups and alkoxy groups of carbon acids 1 to 6.

The stabilized benzimidazole derivative pharmaceutical composition of the present invention is 5% by weight or more (preferably 10% by weight or more, more preferably 10 to 200% by weight or less) with respect to the benzimidazole derivative of the general formula (I). It is characterized by containing a basic organic substance of. Here, the basic organic substance means that the substance is dissolved or suspended in water and has a pH of more than 7, preferably 8 or more.
It is a substance showing the above.

The basic organic substance is preferably a salt of an organic acid with a metal or amine selected from the group consisting of alkali metals, alkaline earth metals or aluminum, amides, basic amino acids, thiamine and amines.

The organic acid used to form the above salt includes
Fatty acids (eg higher fatty acids with 12 to 22 carbon atoms), benzoic acid,
Alginic acid, edetic acid, citric acid, glycyrrhizic acid,
Examples thereof include glutamic acid, gluconic acid, succinic acid, fumaric acid, salicylic acid, and lactic acid. Particularly, higher fatty acids having 12 to 22 carbon atoms such as stearic acid, palmitic acid and myristic acid are preferable.

Examples of alkali metals, alkaline earth metals, aluminum, and amines used to form the above salts include sodium, potassium, calcium, magnesium, aluminum, diisopropanolamine, diphenylamine, ethanolamine, benzylamine. be able to.

Preferred as a salt of an organic acid with a metal or amine selected from the group consisting of alkali metals, alkaline earth metals or aluminum is sodium stearate,
Potassium stearate, magnesium stearate, aluminum stearate, sodium palmitate, potassium palmitate, magnesium palmitate, aluminum palmitate, sodium myristate, potassium myristate, magnesium myristate, aluminum myristate, sodium benzoate, sodium alginate. , Sodium edetate, sodium citrate, sodium glycyrrhizinate, potassium glycyrrhizinate, sodium glutamate, sodium gluconate, potassium gluconate, sodium succinate, sodium fumarate, sodium salicylate and calcium lactate.

Examples of amides are nicotinic acid amide, monomethylnicotinic acid amide, examples of basic amino acids are histidine, examples of thiamine are vitamin-B ₁ , and examples of amines are diisopropanolamine, diphenylamine, ethanolamine, benzylamine. Can be mentioned.

In the pharmaceutical composition of the present invention, the main object of the present invention is that the benzimidazole derivative of the general formula (I) is in the form of particles and is present in the form of fine particles having an average particle size of 10 micro or less. It is desirable to further enhance the storage stability of the benzimidazole derivative.

The fine particles of the benzimidazole derivative can be obtained by, for example, pan mill, attrition mill, screw crusher,
It is carried out by using well-known fine particle powder production equipment such as mechanical micronizers such as ring roller mills and ball mills, jet mills, jet pulsarizers, micronizers, recycling atomizer pulverizers, fluid energy micronizers such as air mills. be able to.

INDUSTRIAL APPLICABILITY The benzimidazole derivative pharmaceutical composition of the present invention is useful in both applications of antiulcer agents and cytoprotective agents, and by oral administration or parenteral administration, prevention of gastric acid secretion, treatment of symptoms associated with excessive gastric acid secretion, and It is useful for the treatment or prevention of gastrointestinal inflammatory diseases that do not depend on gastric acid.

The pharmaceutical (pharmaceutical) composition containing the benzimidazole derivative represented by the general formula (I) as an active ingredient is administered orally or parenterally. Examples of the dosage form of the orally-administered agent include tablets, capsules, powders, and granules. For these preparations, usual excipients,
Disintegrators, binders, lubricants, pigments, diluents and the like are used. As the excipient, glucose, sucrose, lactose, microcrystalline cellulose, etc., as the disintegrator, starch, carboxymethyl cellulose calcium, etc., as the lubricant talc, hydrogenated oil, etc., as the binder hydroxypropyl cellulose, Gelatin, polyvinylpyrrolidone, etc. are used. It should be noted that the classification of the use of each additive described above is for convenience and does not limit the action of each additive.

The dose is usually 500m in terms of active ingredient in adults.
It is less than or equal to g, preferably about 100 μg to 300 mg per day, but it can be increased or decreased depending on the age, symptoms and the like.

Next, the present invention will be described in more detail with reference to Examples and Comparative Examples. The 2- (2-dimethylaminobenzylsulfinyl) benzimidazole used in each example was produced by the following method.

2-mercaptobenzimidazole 4.73 g ethanol 1
After dissolving in 50 ml, 6.18 g of 2-dimethylaminobenzyl chloride.hydrochloride was added and stirred at room temperature for 30 minutes. The precipitated crystals were collected by filtration, saturated NaHCO ₃ solution was added to the crystal cormorants, and extracted with chloroform. The chloroform layer was washed with saturated saline and dried with Glauber's salt. The solvent was distilled off under reduced pressure, and the residue was recrystallized from chloroform-acetonitrile to give 2-
5.39 g of (2-dimethylaminobenzylthio) benzimidazole was obtained as colorless crystals. mp: 164 ° C.

2- (2-Dimethylaminobenzylthio) benzimidazole (4.8 g) was added to chloroform (40 ml) and methanol (5 m).
After dissolving in a mixed solution of 1 and cooling to 0 ° C., 3.86 g of m-chloroperbenzoic acid (purity 70%) was added little by little. After 10 minutes, saturated NaHCO ₃ solution was added to the reaction mixture, and the mixture was extracted with chloroform. The chloroform solution was washed with a saturated saline solution and dried with Glauber's salt. Chloroform was distilled off under reduced pressure, acetonitrile was added to the residue, and the precipitated crystals were collected and 2.97 g of 2-
(2-Dimethylaminobenzylsulfinyl) benzimidazole was obtained as colorless crystals. mp: 116 ° C. (decomposition) [Examples 1 to 3] 1.0 kg of 2- (2-dimethylaminobenzylsulfinyl) benzimidazole colorless crystals was jet-milled 100AS.
(Fuji Sangyo Co., Ltd.) was pulverized with an air flow pressure of 5.5 kg / cm ² at an introduction rate of 1 kg / hour to obtain 95% yield and 2- (2-
Fine crystals of dimethylaminobenzylsulfinyl) benzimidazole (white crystalline powder, decomposition point: 121-127)
C., average particle size: 2 μm) was obtained.

A composition obtained by adding and mixing the basic substance described in Table 1 at a ratio of 1: 1 (weight ratio) to the fine crystals of 2- (2-dimethylaminobenzylsulfinyl) benzimidazole described above was prepared at 50 ° C. and 75 ° C. After storing for 16 days under the condition of% RH, the storage stability was evaluated by measuring the amount of 2- (2-dimethylaminobenzylsulfinyl) benzimidazole remaining in the composition.

In addition, the measurement of the remaining 2- (2-dimethylaminobenzylsulfinyl) benzimidazole was performed by sampling about 900 mg of the sample (the composition after storage), weighing it, and then adding methanol to this and extracting by shaking. While exactly 100 ml
Then, the extract was diluted 100-fold with methanol, and 20 μ of the diluted solution was used to perform quantification according to the HPLC method.

The storage stability test results are shown in Table 1.

Comparative Example 1 The storage stability of 2- (2-dimethylaminobenzylsulfinyl) benzimidazole was evaluated in the same manner as in Example 1 except that the addition of the basic substance was omitted.

The storage stability test results are shown in Table 1.

[Comparative Examples 2 to 9] The storage stability of 2- (2-dimethylaminobenzylsulfinyl) benzimidazole was measured in the same manner as in Example 1 except that the basic substance was changed to the neutral or acidic substance shown in Table 1. evaluated.

The storage stability test results are shown in Table 1.

 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mitsuko Yoshioka 1372 Hiranuma, Yoshikawa-cho, Kita-Katsushika-gun, Saitama Prefecture (72) Terumasa Moriga 4-14-712 Hikonari, Misato City, Saitama (56) Reference JP 62 -283964 (JP, A)

Claims (10)

[Claims] 1. General formula (I): (In the formula, R ¹ represents a hydrogen atom, an alkyl group having 1 to 8 carbon atoms, a cycloalkyl group, a phenyl group or an aralkyl group, and R ² represents a hydrogen atom or a lower alkyl group, or R ¹ and R 2 ² together form a ring with an adjacent nitrogen atom, and R ³ and R ⁴ are each independently a hydrogen atom, a halogen atom, a trifluoromethyl group, a lower alkyl group, a lower alkoxy group, a lower alkoxycarbonyl group or A stabilized benzimidazole derivative pharmaceutical composition comprising a benzimidazole derivative having an amino group) having a physiological activity and 5% by weight or more of a basic organic substance with respect to the benzimidazole derivative. object. 2. The basic organic substance is a salt of an organic acid with a metal or amine selected from the group consisting of alkali metals, alkaline earth metals or aluminum, an amide, a basic amino acid, thiamine or an amine. The benzimidazole derivative pharmaceutical composition according to claim 1. 3. The benzimidazole derivative pharmaceutical composition according to claim 1, wherein the basic organic substance is a salt of an alkali metal or alkaline earth metal and a higher fatty acid. 4. The benzimidazole derivative pharmaceutical composition according to claim 1, wherein the basic organic substance is contained in an amount of 10% by weight or more based on the benzimidazole derivative. 5. The benzimidazole derivative pharmaceutical composition according to claim 1, wherein the basic substance is contained in an amount of 10 to 200% by weight based on the benzimidazole derivative. 6. The benzimidazole derivative pharmaceutical composition according to claim 1, wherein the benzimidazole derivative in the composition is in the form of particles and has an average particle size of 10 μm or less. 7. A general formula (I) of a benzimidazole derivative.
The benzimidazole derivative pharmaceutical composition according to claim 1, wherein R ^{1 in} is an alkyl group having 1 to 8 carbon atoms. 8. A general formula (I) of a benzimidazole derivative.
Wherein R ^{2 in} is a lower alkyl group.
A benzimidazole derivative pharmaceutical composition according to the above item. 9. A general formula (I) of a benzimidazole derivative.
The benzimidazole derivative pharmaceutical composition according to claim 1, wherein R ^{3 in} is a hydrogen atom or a lower alkyl group. 10. The benzimidazole derivative pharmaceutical composition according to claim 1, wherein R ⁴ in the general formula (I) of the benzimidazole derivative is a hydrogen atom or a lower alkyl group.