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2-CYCLOAMINO-5-(PYRIDIN-4-YL)IMIDAZO2,1-B1,3,4THIADIAZOLE DERIVATIVES, PREPARATION THEREOF, AND THERAPEUTIC USE THEREOF
2-CYCLOAMINO-5-(PYRIDIN-4-YL)IMIDAZO2,1-B1,3,4THIADIAZOLE DERIVATIVES, PREPARATION THEREOF, AND THERAPEUTIC USE THEREOF
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机译:2-环氯氨基-5-(吡啶-4-基)咪唑并[2,1- B I>] [1,3,4]噻二唑衍生物,其制备和治疗用途
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摘要
The invention relates to 2-cycloamino-5-(pyridin-4-yl)imidazo[2,1-b][1,3,4]thiadiazole derivatives of the general formula (I) where: R5 is a hydrogen atom or a C1-3 alkyl, -NR7R8, or C1-3 alkyloxy group; R6 is an optionally substituted phenyl group; A is a C1-7-alklene group optionally substituted by one or two Ra groups; B is a C1-7-alkylene group optionally substituted by an Rb group; L is a nitrogen atom optionally substituted by an Rc or Rd group, or a carbon atom substituted by a Rei group and a Rd group or two Re2 groups; R7 and R8 are independently a hydrogen atom or a C1-3 alkyl group. The invention also relates to a method for preparing same and to the therapeutic use thereof.
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机译:本发明涉及通式(I)的2-环氨基-5-(吡啶-4-基)咪唑并[2,1- b I>] [1,3,4]噻二唑衍生物,其中: R5是氢原子或C 1-3 Sub>烷基,-NR 7 Sub> R 8 Sub>或C 1-3 Sub>烷氧基; R6是任选取代的苯基; A为任选被一个或两个R a Sub>基团取代的C 1-7 Sub>-烯基; B是任选地被R b Sub>基团取代的C 1-7 Sub>-亚烷基; L是被R c Sub>或R d Sub>基团任选取代的氮原子,或被Rei基和R d Sub>基团取代的碳原子。组或两个R e2 Sub>组; R 7 Sub>和R 8 Sub>独立地是氢原子或C 1-3 Sub>烷基。本发明还涉及其制备方法及其治疗用途。
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