申请人:Gruppo Lepetit, S.p.A.
公开号:US04007276A1
公开(公告)日:1977-02-08
New s-triazolo[5,1-a]isoindole derivatives of following formula I ##STR1## wherein R is selected from hydrogen, amino, lower alkyl amino, di-lower alkyl amino, acylamino, diacylamino, benzoylamino, ureido, thioureido, carbethoxythioureido, benzoylthioureido, sulfhydryl, lower alkyl, trifluoromethyl, phenyl, substituted phenyl, pyridyl, methylpyridyl and dimethylpyridyl; and R.sub.1 and R.sub.2 each independently represents hydrogen, chloro or lower alkoxy. A process for their manufacture which comprises the reaction of 2-aminophthalimidine with a reagent R-Z wherein R has the same meaning as above, and Z represents one of the following groups: ##STR2## wherein R.sub.3 is C.sub.1 -C.sub.4 alkyl. The compounds and some of the intermediates of the process are useful as antiinflammatories, analgesics, CNS depressants, antimicrobials and anti-fertility agents.
新型s-三唑并[5,1-a]异吲哚衍生物,其具有以下通式I ##STR1## 其中R选自氢、氨基、低级烷基氨基、二低级烷基氨基、酰胺基、二酰胺基、苯甲酰胺基、脲基、硫脲基、乙氧羰基硫脲基、苯甲酰硫脲基、巯基、低级烷基、三氟甲基、苯基、取代苯基、吡啶基、甲基吡啶基和二甲基吡啶基;且R1和R2各自独立地表示氢、氯或低级烷氧基。其制备方法包括2-氨基邻苯二甲酰亚胺与试剂R-Z反应,其中R具有上述含义,Z表示以下组之一: ##STR2## 其中R3是C1-C4烷基。该化合物及该方法的一些中间体可作为抗炎剂、镇痛剂、中枢神经系统抑制剂、抗微生物剂和抗生育剂使用。