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Heterocyclically substituted imidazolidines, processes and intermediates for their preparation, their use as medicaments and pharmaceutical preparations containing them
Heterocyclically substituted imidazolidines, processes and intermediates for their preparation, their use as medicaments and pharmaceutical preparations containing them
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机译:杂环取代的咪唑烷类,其制备方法和中间体,其用作包含它们的药物和药物制剂的用途
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摘要
Imidazolidines of formula (I) in racemic, enantiomeric and diasteroisomeric forms, and their salts are new. In (I) ring is e.g. satd. heterocycle of 4-7 members contg. either O, N, S (opt. oxidised), and opt. substd. by a group selected from R3; Ar is e.g. aryl (opt. substd. by halo, CN, NO2, CF3, CF3O, OH, COOH or salified, esterified, or amidified COOH) or a gp. (ii) in which N is opt. oxidised and R1 and R2 are H or (substd.) alkyl, or form with N atom e.g. 5, 6 or 7 membered monocyclic ring opt. contg. other heteroatoms (O, N, S) and opt. substd. etc.; X is O or S; Y is O, S or NH; R3 is H, aryl, alkyl, alkenyl, alkynyl, opt. interrupted by one or more O, N, or S (opt. oxidised) atoms, and opt. substd.
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机译:外消旋,对映异构和非对映异构形式的式(I)的咪唑烷及其盐是新的。在(I)中,环为例如。坐下4-7个成员的杂环续O,N,S(氧化)和opt。取代从R3中选择的一个组; Ar是例如芳基(由卤素,CN,NO2,CF3,CF3O,OH,COOH或成盐,酯化或酰胺化的COOH取代)或gp。 (ii)N是最佳选择。被氧化的R 1和R 2是H或(被取代的)烷基,或与N原子形成如5、6或7元单环环。续其他杂原子(O,N,S)并选择。取代等等。; X是O或S; Y为O,S或NH; R 3是H,芳基,烷基,烯基,炔基,opt。被一个或多个O,N或S(最佳氧化)原子打断,并且取代
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