Salts of benzimidazole derivative with amines and process for manufacturing the same

a technology of benzimidazole and amines, which is applied in the field of salts of benzimidazole derivatives with amines and process for manufacturing the same, can solve the problems of ineffective crystallization process of salts of compounds such as omeprazole that act as proton pump inhibitors with amines, and no method of obtaining alkali metal salts, etc., and achieves efficient removal

Inactive Publication Date: 2009-10-22
YOKOI HIROYUKI +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0020]According to the present invention, the sulfone contained as an impurity can be efficiently removed by using salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole with amines when manufacturing 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole, which is useful as a drug.

Problems solved by technology

The crystallization process of salts of compounds such as omeprazole that act as proton pump inhibitors with amines is also not known to be useful for removing impurities and the like.
Moreover, no method is known of obtaining alkali metal salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole from salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole with amines.

Method used

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  • Salts of benzimidazole derivative with amines and process for manufacturing the same
  • Salts of benzimidazole derivative with amines and process for manufacturing the same
  • Salts of benzimidazole derivative with amines and process for manufacturing the same

Examples

Experimental program
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Effect test

reference example 1

[0097]2-Hydroxymethyl-4-(3-methoxypropoxy)-3-methylpyridine (5.0 g (23.7 mmol)) was dissolved in toluene (40 ml), and thionyl chloride (4.23 g (35.6 mmol)) was added dropwise thereto so that the temperature did not exceed 25° C. Following stirring at room temperature, disappearance of the raw materials was confirmed by TLC, and 2-chloromethyl-4-(3-methoxypropoxy)-3-methylpyridine (6.13 g) was obtained by concentrating under a reduced pressure (yield: 97.3%).

reference example 2

[0098]2-Hydroxymethyl-4-(3-methoxypropoxy)-3-methylpyridine (5.0 g (23.7 mmol)) was dissolved in ethyl acetate (40 ml), and thionyl chloride (4.23 g (35.6 mmol)) was added dropwise thereto so that the temperature did not exceed 25° C. Following stirring at room temperature, disappearance of the raw materials was confirmed by TLC, and 2-chloromethyl-4-(3-methoxypropoxy)-3-methylpyridine (6.14 g) was obtained by concentrating under a reduced pressure (yield: 97.4%).

reference example 3

[0099]2-Hydroxymethyl-4-(3-methoxypropoxy)-3-methylpyridine (5.0 g (23.7 mmol)) was dissolved in dimethoxyethane (40 ml), and thionyl chloride (4.23 g (35.6 mmol)) was added dropwise thereto so that the temperature did not exceed 25° C. Following stirring at room temperature, disappearance of the raw materials was confirmed by TLC, and 2-chloromethyl-4-(3-methoxypropoxy)-3-methylpyridine (6.25 g) was obtained by concentrating under a reduced pressure (yield: 99.2%).

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Abstract

It is an object of the present invention to provide (1) a process for manufacturing alkali metal salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole which are useful as gastric acid secretion inhibitors, anti-ulcer agents and other drugs and (2) salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole with amines which are intermediates for the production of the alkali metal salts, and a process for manufacturing the same. According to the present invention, disclosed are salts represented by the following formula (I):(wherein A+ represents an isopropylammonium ion, sec-butylammonium ion or cyclopentylammonium ion).

Description

[0001]This application is a Divisional application which priority is claimed under 35 U.S.C. § 120 to U.S. application Ser. No. 11 / 632,931 filed on Jan. 19, 2007. Application Ser. No. 11 / 632,931 is the national phase of PCT International Application No. PCT / JP2005 / 014400 filed on Aug. 5, 2005 and claims priority under 35 U.S.C. § 119(a) to Patent Application No. 2004-230094 filed in Japan on Aug. 6, 2004, all of which are hereby expressly incorporated by reference, into the present application.TECHNICAL FIELD[0002]The present invention relates to (1) a process for manufacturing alkali metal salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole which are useful as gastric acid secretion inhibitors, anti-ulcer agents and other drugs and (2) salts of 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole with amines which are intermediates for the production of the alkali metal salts, and a process for manufacturing them.BACKGRO...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07D401/12
CPCC07D401/12A61P1/00A61P1/02A61P1/04
Inventor YOKOI, HIROYUKIMIZUNO, MASANORIHAGA, TOYOKAZU
Owner YOKOI HIROYUKI
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