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Derivatives of (1,2,4) triazolo 4,3-a quinoxaline inhibitors of phosphodiesterases

机译:磷酸二酯酶的(1,2,4)三唑并[4,3-a]喹喔啉抑制剂的衍生物

摘要

Relating to compounds of formula (i) wherein: R1 is piridilo phenyl 2 -, 3 - or 4 - piridilo piridilo, which are replaced with different Substituent in Ortho position of H a ligation to the structure of the main Chain; R2 is H, c1-c4 alkyl, optionally substituted with up to 2 halo ; R3, R4, R5 and R6 are independently h, halogen, CN, oC1-c4 alkyl, optionally substituted with up to 5 Halo, among others. Preferred compounds are: 8 - chlorine - 1 - (2 - chloro phenyl) - 4 - methyl - [1,2,4] triazolo [4,3-a] quinoxaline; 4-chloro-3 - (8 - chlorine - 4 - methyl - [1,2,4] triazolo [4,3-a] quinoxalin - 1 - il) phenol, among others.These compounds are inhibitors of phosphodiesterase 2 and / or 10, be helpful for the treatment of Alzheimer's disease, Mental Retardation, Neurotic disorders, Schizophrenia, Epilepsy
机译:关于式(i)的化合物,其中:R1是吡啶子基苯基2-,3-或4-吡啶子基哌啶子基,其在H的邻位被不同的取代基取代成与主链的结构连接; R 2是H,c 1 -c 4烷基,任选被至多2个卤素取代; R 3,R 4,R 5和R 6独立地是h,卤素,CN,oC 1 -c 4烷基,任选地被至多5个卤素取代。优选的化合物是:8-氯-1-(2-氯苯基)-4-甲基-[1,2,4]三唑并[4,3-a]喹喔啉;其中包括4-氯-3-(8-氯-4-甲基-[1,2,4]三唑[4,3-a]喹喔啉-1-il)苯酚。这些化合物是磷酸二酯酶2和/或10,有助于治疗阿尔茨海默氏病,智力低下,神经性疾病,精神分裂症,癫痫

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