发明名称 AMIDINE DERIVATIVES OF 2-SUBSITUTED 4-PHENYL IMIDAZOLE
摘要 Object of the present invention are new pharmacologically active amidine derivatives of 2-substituted 4-phenylimidazole of formula …<CHEM>… in which R representa a linear or branched alkyl group, a hydroxy group, a C1-3 alkoxy group, a mercapto group, C1-3 alkylthio group, a halogen atom, a C1-3 alkylsulfinyl or alkylsulfonyl group, a sulfamoyl group, an amino group which may be substituted by one or two alkyl groups having 1 to 3 carbon atoms, an acylamino group or a phenyl group; R1 and R2, which may be the same or different, represent a hydrogen atom or an alkyl group; R3 represents a linear or branched alkyl group containing optionally one heteroatom such as an oxygen, a sulphur or a nitrogen atom, an alkenyl group, an alkynyl group, a cyano group, an aryl or an aralkyl group optionally substituted, a cycloalkyl or cycloaliphatic alkyl group, a substituted or unsubstituted heterocyclilalkyl or heterocyclic group; R4 represents a hydrogen atom, a C1-3 alkyl or alkoxy group, a halogen atom, a cyano or carbamoyl group, tautomeric forms thereof and acid addition salts thereof. …<??>Processes for the preparation of the compounds of formula (1) and their intermediates as well as the pharmaceutical compositions containing them are also object of this invention. …<??>The new compounds are H2-receptor blocking agents which inhibit the gastric acid secretion and are useful antiulcer agents.
申请公布号 AU565292(B2) 申请公布日期 1987.09.10
申请号 AU19840030800 申请日期 1984.07.18
申请人 ISTITUTO DE ANGELI S.P.A. 发明人 GIUSEPPE BIETTI;ENZO CEREDA;ARTURO DONETTI;ANTONIO GIACHETTI;FERDINANDO PAGANI
分类号 C07D233/34;A61K31/415;A61K31/4164;A61K31/4166;A61P1/04;C07D233/54;C07D233/64;C07D233/66;C07D233/68;C07D233/70;C07D233/84;C07D233/88 主分类号 C07D233/34
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