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Pyridoindolone derivatives substituted in the 3-position by a heterocyclic group, their preparation and their application in therapeutics
Pyridoindolone derivatives substituted in the 3-position by a heterocyclic group, their preparation and their application in therapeutics
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机译:在3位上被杂环基取代的吡啶并吲哚酮衍生物及其制备方法和在治疗中的应用
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摘要
The present invention relates to pyridoindolone derivatives substituted in the 3-position by a heterocyclic group of general formula (I):; in which:R1 represents a hydrogen atom or a (C1-C4)alkyl group;R2 represents a hydrogen atom or a (C1-C4)alkyl group;R3 represents a thienyl mono- or polysubstituted by a methyl group; or a monocyclic or bicyclic heterocyclic radical chosen from: a pyridyl, an N-oxidopyridinio, a pyrazolyl, an (N-phenyl)pyrazolyl, an (N-halophenyl)pyrazolyl, a furyl, an indolyl, an (N-benzyl)indolyl, an (N-halobenzyl)indolyl, a benzothienyl or a benzofuryl, the said radicals being unsubstituted or substituted one or more times by a halogen atom or a methyl or methoxy group;R4 and R5 are identical or different and each independently represent a hydrogen or halogen atom or a hydroxyl, hydroxymethyl, (C1-C4)alkyl, trifluoromethyl, C1-C4)alkoxy, (C1-C4)alkoxycarbonyl or cyano group.;Preparation process and application in therapeutics.
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机译:本发明涉及在3-位被通式(Ⅰ)的杂环基取代的吡啶并吲哚酮衍生物: 化学>其中: R 1 Sub>表示氢原子或(C 1 Sub> -C 4 Sub>)烷基; ListItem> < ListItem id =“ ul0002-0002” number =“ 0000”> R 2 Sub>表示氢原子或(C 1 Sub> -C 4 Sub>)烷基; ListItem> R 3 Sub>表示被甲基单或多取代的噻吩基;或选自以下的单环或双环杂环基团:吡啶基,N-氧化吡啶基,吡唑基,(N-苯基)吡唑基,(N-卤代苯基)吡唑基,呋喃基,吲哚基,(N-苄基)吲哚基,(N-卤代苄基)吲哚基,苯并噻吩基或苯并呋喃基,所述基团未被取代或被卤素原子或甲基或甲氧基取代一次或多次; ListItem> R 4 Sub>和R 5 Sub>相同或不同,分别独立地表示氢或卤素原子或羟基,羟甲基(C 1 Sub> -C 4 Sub>)烷基,三氟甲基,C 1 Sub> -C 4 Sub>)烷氧基,(C 1 Sub > -C 4 Sub>)烷氧羰基或氰基。 ListItem> UnorderedList> ListItem> UnorderedList>;制备工艺及在治疗中的应用。
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