Process of producing guanidinothiazole derivatives
AssigneeYamanouchi Pharmaceutical Co., Ltd.
InventorsYoshio Ishii, Isao Yanagisawa
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Abstract
A process is provided for producing a guanidinothiazole compound represented by the formula: ##STR1## wherein, R.sup.1 and R.sup.2, which may be the same or different, each represents a hydrogen or an alkyl group having 1 to 3 carbon atoms; m represents 1 or 2; and n represents 2, 3 or 4. The process comprises reacting an aminothiazole compound of the formula: ##STR2## with a cyanamide or an amidinopyrazole, the compounds are useful as intermediates in the preparation of a gastric acid secretion inhibitor.
Claims4
A process of producing a guanidinothiazol compound of the formula ##STR11## wherein R.sup.1 and R.sup.2, which may be the same or different, each represents a hydrogen or an alkyl group having 1 to 3 carbon atoms;
- m represents 1 or 2;
- and n represents 2, 3 or 4, or an acid addition salt thereof, which comprises reacting in the presence of a Lewis acid catalyst, an aminothiazol compound represented by the formula:
- ##STR12## wherein R.sup.1, m and n have the same values as defined above, or an acid addition salt and an amidinopyrazole compound represented by the formula:
- ##STR13## wherein R.sup.3 and R.sup.4, which may be the same or different, each represents a hydrogen atom or an alkyl group having 1 to 3 carbon atoms and R.sup.2 has the same value as defined above, said reaction being effected in a high-boiling solvent at a temperature of at least 100.degree. C. and wherein said Lewis acid catalyst is selected from the group consisting of zinc oxide, zinc chloride, copper (I) chloride and aluminum chloride, and thereafter recovering said guanidinothiazole.
Dependencies are inferred from the claim text.