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N-oxide and/or di-n-oxide derivatives of dopamine receptor stabilizers/modulators displaying improved cardiovascular side-effects profiles

机译:多巴胺受体稳定剂/调节剂的N-氧化物和/或Di-N-氧化物衍生物显示出改善的心血管副作用

摘要

A compound having the general formula wherein A is selected from the group consisting of to the formation of a compound of the general formula (1) and a compound of the general formula (2) respectively, and pharmaceutically acceptable salts thereof, wherein R1 is a member selected from the group consisting of CF3, OSO2CF3, OSO2CH3, SOR4, SO2R4, COR4, CN, OR4, NO2, CONHR4, 3-thiophene, 2-thiophene, 3-furane, 2-furane, F, Cl, Br and I, wherein R4 is as defined below; R2 is a member selected from the group consisting of H, F, Cl, Br, I, CN, CF3, CH3, OCH3, OH, NH2, SOmCF3, O(CH2)mCF3, SO2N(R4)2, CHNOR4, COCOOR4, COCOON(R4)2, (C1-C8)alkyl, (C3-C8)cykloalkyl, CH2OR4, CH2(R4)2, NR4SO2CF3, NO2, at phenyl at positions 2, 4, 5 or 6, wherein x and R4 are as defined below; R3 is a member selected from the group consisting of hydrogen, CF3, CH2CF3, (C1-C8)alkyl, (C3-C8)cykloalkyl, (C4-C9)cycloalkylmethyl, (C2-C8)alkenyl, (C2-C8)alkynyl, 3,3,3-tri-fluoropropyl, 4,4,4-trifluorobutyl, CH2SCH3, CH2CH2OCH3, CH2CH2CH2F, CH2CF3, phenylethyl, 2-thiopheneethyl and 3-thiopheneethyl; R4 is a member selected from the group consisting of hydrogen, CF3, CH2CF3, (C1-C8)alkyl, (C3-C8)cycloalkyl, (C4-C9)cycloalkylmethyl, (C2-C8)alkenyl, (C2-C8)alkynyl, 3,3,3-trifluoropropyl, 4,4,4-trifluorobutyl, 2-tetrahydrofurane and 3-tetrahydrofurane; X is selected from the group consisting of N and sp3-hybridized C; Y is selected from the group consisting of O and, when R3 represents H, OH; Z is selected from the group consisting of H and OH when X is sp3-hybridized C or Z represents O or an electronic lone-pair when X is N; the dashed line represents a bond when X is sp2-hybridized C or is absent when X is N; m is an integer 1 or 2; n is an integer 1-3; provided that when n in Formula 1 is 2, R1 is SO2CH3 and R2 is H R3 does not represent n-propyl. The invention also relates to a pharmaceutical preparation containing said compound, the use of said compound for the manufacture of a pharmaceutical composition and a method for the treatment of a disorder in the central nervous system of a patient using said compound.
机译:具有通式(其中A选自分别形成通式(1)的化合物和通式(2)的化合物)及其药学上可接受的盐的通式的化合物,其中R 1是A选自CF3,OSO2CF3,OSO2CH3,SOR4,SO2R4,COR4,CN,OR4,NO2,CONHR4、3-噻吩,2-噻吩,3-呋喃,2-呋喃,F,Cl,Br和I的成员,其中R4如下定义; R 2是选自H,F,Cl,Br,I,CN,CF3,CH3,OCH3,OH,NH2,SOmCF3,O(CH2)mCF3,SO2N(R4)2,CHNOR4,COCOOR4的成员位置2、4、5或6的苯基上的COCOON(R4)2,(C1-C8)烷基,(C3-C8)环烷基,CH2OR4,CH2(R4)2,NR4SO2CF3,NO2,其中x和R4为定义如下; R 3是选自氢,CF 3,CH 2 CF 3,(C 1 -C 8)烷基,(C 3 -C 8)环烷基,(C 4 -C 9)环烷基甲基,(C 2 -C 8)烯基,(C 2 -C 8)炔基的成员。 ,3,3,3-三氟丙基,4,4,4-三氟丁基,CH2SCH3,CH2CH2OCH3,CH2CH2CH2F,CH2CF3,苯乙基,2-噻吩乙基和3-噻吩乙基; R4是选自氢,CF3,CH2CF3,(C1-C8)烷基,(C3-C8)环烷基,(C4-C9)环烷基甲基,(C2-C8)烯基,(C2-C8)炔基的成员,3,3,3-三氟丙基,4,4,4-三氟丁基,2-四氢呋喃和3-四氢呋喃; X选自N和sp3-杂化的C; Y选自由O组成的组,并且当R 3代表H时,OH;和当X是sp3-杂化的C时,Z选自由H和OH组成的组;当X是N时,Z代表O或电子孤对。虚线表示当X为sp2-杂化的C时的键或当X为N时的键不存在。 m是1或2的整数; n为1-3的整数;假设式1中的n为2时,R 1为SO 2 CH 3且R 2为H R 3不代表正丙基。本发明还涉及含有所述化合物的药物制剂,所述化合物在制备药物组合物中的用途,以及使用所述化合物治疗患者中枢神经系统疾病的方法。

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