N-Substituted-3-arylpyrrolidines: Potent and selective ligands at serotonin 1A receptor
摘要:
3-Arylpyrrolidines are synthesized through the coupling of N-benzyl-3-(methanesulfonyloxy)pyrrolidine with diarylcuprates. Pharmacological evaluation of a series of N-substituted-3-arylpyrrolidines toward several neurotransmitter receptors indicated that some of them are good ligands for serotonin 1A receptor. Particularly, N-[(N-saccharino)butyl]pyrrolidines were found to be potent and selective ligands. A preliminary biological evaluation for several selected compounds indicated that they are potentially effective antianxiety and antidepressant agents. (C) 1999 Elsevier Science Ltd. All rights reserved.
DOI:
10.1016/s0960-894x(99)00201-2
作为产物:
描述:
哌啶 、 3-(bromomethyl)benzoyl bromide 在
ice 、 乙酸乙酯 、 hexanes 作用下,
以
苯 为溶剂,
反应 3.0h,
以to give the titled compound as a clear oil (578 mg, 41% yield)的产率得到(3-(bromomethyl)phenyl)(piperidin-1-yl)methanone
Compounds, pharmaceutical compositions, kits, article of manufacture, methods of using, and method of preparing of compounds having the formula of:
wherein the variables are as defined herein.
[EN] RENIN INHIBITORS<br/>[FR] INHIBITEURS DE RÉNINE
申请人:TAKEDA PHARMACEUTICAL
公开号:WO2008089005A2
公开(公告)日:2008-07-24
[EN] Compounds, pharmaceutical compositions, kits, article of manufacture, methods of using, and method of preparing of compounds having the formula of : wherein the variables are as defined herein. [FR] L'invention concerne des composés, des compositions pharmaceutiques, des trousses, des articles de fabrication, des procédés d'utilisation, et des procédés de préparation de composés ayant la formule : dans laquelle les variables sont telles que définies ici.
N-Substituted-3-arylpyrrolidines: Potent and selective ligands at serotonin 1A receptor
作者:Kyo Han Ahn、Seok Jong Lee、Chang-Ho Lee、Chang Y. Hong、Tae Kyo Park
DOI:10.1016/s0960-894x(99)00201-2
日期:1999.5
3-Arylpyrrolidines are synthesized through the coupling of N-benzyl-3-(methanesulfonyloxy)pyrrolidine with diarylcuprates. Pharmacological evaluation of a series of N-substituted-3-arylpyrrolidines toward several neurotransmitter receptors indicated that some of them are good ligands for serotonin 1A receptor. Particularly, N-[(N-saccharino)butyl]pyrrolidines were found to be potent and selective ligands. A preliminary biological evaluation for several selected compounds indicated that they are potentially effective antianxiety and antidepressant agents. (C) 1999 Elsevier Science Ltd. All rights reserved.