首页> 外国专利> USE OF SULPHONAMIDE DERIVATIVES FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITIONS POTENTIATING GLUTAMATE RECEPTOR FUNCTION

USE OF SULPHONAMIDE DERIVATIVES FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITIONS POTENTIATING GLUTAMATE RECEPTOR FUNCTION

机译:使用磺酰胺衍生物制备潜在的谷氨酸受体功能的药物组合物

摘要

The present invention relates to the use of a compound of formula (I) or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for enhancing glutamate receptor function. Compounds of general formula (Ia) represented by the general formula (I) are novel and are also within the scope of the invention. The invention also relates to pharmaceutical compositions containing the compounds of formula (Ia), and also to a process for the preparation of the compounds of formula (Ia), which is a narrower group of compounds of formula (Ia). In the general formulas, the substituents are defined as many, for example, R1 is an optionally substituted aromatic or heteroaromatic group, R2 is C1-6alkyl, C3-6cycloalkyl, C1-6-fluoroalkyl, C1-6 chloro. alkyl, C 2-6 alkenyl, (C 1 -C 4) alkoxy (C 1 -C 4) alkyl, phenyl optionally substituted with halogen, C 1-4 alkyl or C 1-4 alkoxy, or R 3 R 4 N wherein R3 and R4 are independently C1-C4 alkyl or together with the nitrogen atom to which azetidinyl, pyrrolidinyl, piperidinyl, morpholino, piperazinyl, hexahydro-azepinyl or octahydroazocinyl are attached; L is C 2 -C 4 alkylene optionally substituted with one or two C 1-6 alkyl, aryl (C 1-6) alkyl, C 2-6 alkenyl, aryl (C 2 -C 6) alkenyl, and aryl. or the C 2-4 alkylene group may have two substituents which, together with the atom or carbon atoms to which they are attached, form a 3-8 carbon atoms carbocyclic ring, R 14 is an optionally substituted phenyl group. The compounds of formula (I) or pharmaceutically acceptable salts thereof may be used for the treatment and prevention of detection disorders, neurodegenerative diseases, dementia of the elderly, memory deterioration, disorders of movement, depression, attention deficit disorders, psychosis-related disorders. HE
机译:本发明涉及式(I)化合物或其药学上可接受的盐在制备用于增强谷氨酸受体功能的药物中的用途。由通式(I)表示的通式(Ia)的化合物是新颖的,并且也在本发明的范围内。本发明还涉及包含式(Ia)的化合物的药物组合物,并且还涉及式(Ia)的化合物的制备方法,所述式(Ia)的化合物是式(Ia)的一小部分化合物。在通式中,取代基被定义为许多,例如,R 1是任选取代的芳族或杂芳族基团,R 2是C 1-6烷基,C 3-6环烷基,C 1-6-氟烷基,C 1-6氯。烷基,C 2-6烯基,(C 1 -C 4)烷氧基(C 1 -C 4)烷基,任选被卤素取代的苯基,C 1-4烷基或C 1-4烷氧基或R 3 R 4 N,其中R3和R4独立地是C1-C4烷基,或与氮杂环丁烷基,吡咯烷基,哌啶基,吗啉代,哌嗪基,六氢-pin庚基或八氢偶氮基相连的氮原子; L为任选地被一个或两个C 1-6烷基,芳基(C 1-6)烷基,C 2-6烯基,芳基(C 2 -C 6)烯基和芳基取代的C 2 -C 4亚烷基。或C 2-4亚烷基可具有两个取代基,它们与它们所连接的原子或碳原子一起形成3-8个碳原子的碳环,R 14是任选取代的苯基。式(I)化合物或其药学上可接受的盐可用于治疗和预防检测障碍,神经退行性疾病,老年人痴呆,记忆力减退,运动障碍,抑郁症,注意力缺陷障碍,精神病相关障碍。他

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