1-cyclohexanesulfonyl-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-5-nitro-1H-indole 在
钯 作用下,
以
乙醇 为溶剂,
反应 20.0h,
以150 mg (40%) of the mentioned compound were obtained as a solid cream的产率得到5-amino-1-cyclohexanesulfonyl-3-(1-methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole
参考文献:
名称:
1-Sulfonylindole derivatives, their preparation and their use as 5-ht6 ligands
[EN] ACTIVE SUBSTANCE COMBINATION COMPRISING A COMPOUND WITH NPY RECEPTOR AFFINITY AND A COMPOUND WITH 5-HT6 RECEPTOR AFFINITY<br/>[FR] COMBINAISON DE SUBSTANCES ACTIVES COMPORTANT UN COMPOSE A AFFINITE DE RECEPTEUR NPY ET UN COMPOSE A AFFINITE DE RECEPTEUR 5-HT6
申请人:ESTEVE LABOR DR
公开号:WO2005014000A1
公开(公告)日:2005-02-17
The present invention relates to an active substance combination comprising at least one compound with neuropeptide Y-receptor affinity and at least one compound with 5-HT6 receptor affinity, a medicament comprising said active substance combination, and the use of said active substance combination for the manufacture of a medicament.
[EN] 1-SULFONYLINDOLE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS 5-HT6 LIGANDS<br/>[FR] DERIVES DE 1-SULFONYLINDOLE, LEUR PREPARATION ET LEUR UTILISATION EN TANT QUE LIGANDS DE 5-HT6
申请人:ESTEVE LABOR DR
公开号:WO2005013974A1
公开(公告)日:2005-02-17
The present invention refers to new sulfonamide derivatives, of general formula (la, lb, 1c), (I) ,(1 a, I b, I c), optionally in form of one of their stereoisomers, preferably enantiomers or diastereomers, their racemate, or in form of a mixture of at least two of their stereoisomers, preferably enantiomers or diastereomers, in any mixing ratio, or their salts, preferably their corresponding physiologically acceptable salts or corresponding solvates; to the processes for their preparation, to their application as medicaments in human and/or veterinary therapeutics, and to the pharmaceutical compositions containing them. The new compounds of the present invention can be used in the pharmaceutical industry as intermediates and for preparing medicaments.
本发明涉及新的磺酰胺衍生物,其一般式为(la, lb, 1c), (I) ,(1 a, I b, I c),可选地为它们的立体异构体之一,优选为对映异构体或非对称异构体,它们的外消旋体,或者为至少两个它们的立体异构体的混合物,优选为对映异构体或非对称异构体,在任何混合比例下,或它们的盐,优选为相应的生理可接受的盐或相应的溶剂化合物;还涉及它们的制备方法,它们在人类和/或兽医治疗中作为药物的应用,以及含有它们的制药组合物。本发明的新化合物可用于制药工业中的中间体和制备药物。
Active substance combination comprising a compound with npy receptor affinity and a compound with 5-ht6 receptor affinity
申请人:Torrens Jover Antoni
公开号:US20070009597A1
公开(公告)日:2007-01-11
The present invention relates to an active substance combination comprising at least one compound with neuropeptide Y-receptor affinity, preferably neuropeptide Y5-receptor affinity, and at least one compound with 5-HT
6
receptor affinity, a medicament comprising said active substance combination, and the use of said active substance combination for the manufacture of a medicament.
1-Sulfonylindole derivatives, their preparation and their use as 5-ht6 ligands
申请人:Merce Vidal Ramon
公开号:US20070060581A1
公开(公告)日:2007-03-15
The present invention refers to new sulfonamide derivatives, of general formula (Ia, Ib, Ic), (I), (Ia, Ib, Ic), optionally in form of one of their stereoisomers, preferably enantiomers or diastereomers, their racemate, or in form of a mixture of at least two of their stereoisomers, preferably enantiomers or diastereomers, in any mixing ratio, or their salts, preferably their corresponding physiologically acceptable salts or corresponding solvates; to the processes for their preparation, to their application as medicaments in human and/or veterinary therapeutics, and to the pharmaceutical compositions containing them. The new compounds of the present invention can be used in the pharmaceutical industry as intermediates and for preparing medicaments.
1-sulfonylindole derivatives, their preparation and their use as 5-HT6 ligands
申请人:Laboratorios del Dr. Esteve S.A.
公开号:US07655690B2
公开(公告)日:2010-02-02
The present invention refers to new sulfonamide derivatives, of general formula (Ia, Ib, Ic), (I), (Ia, Ib, Ic), optionally in form of one of their stereoisomers, preferably enantiomers or diastereomers, their racemate, or in form of a mixture of at least two of their stereoisomers, preferably enantiomers or diastereomers, in any mixing ratio, or their salts, preferably their corresponding physiologically acceptable salts or corresponding solvates; to the processes for their preparation, to their application as medicaments in human and/or veterinary therapeutics, and to the pharmaceutical compositions containing them. The new compounds of the present invention can be used in the pharmaceutical industry as intermediates and for preparing medicaments.