[EN] (DIHYDRO) IMIDAZOISO (5, 1-A) QUINOLINES AS FSH RECEPTOR AGONISTS FOR THE TREATMENT OF FERTILITY DISORDERS<br/>[FR] (DIHYDRO)IMIDAZO-ISO(5,1-A)QUINOLÉINES EN TANT QU'AGONISTES DU RÉCEPTEUR DE LA FSH POUR LE TRAITEMENT DE TROUBLES DE LA FERTILITÉ
申请人:ORGANON NV
公开号:WO2010136438A1
公开(公告)日:2010-12-02
The invention relates to imidazoiso[5,1-a]quinoline and 5,6-dihydro-imidazoiso[5,1-a]quinoline derivatives according to general Formula (1) or a pharmaceutically acceptable salt thereof. The compounds can be used for the treatment of infertility.
(DIHYDRO)IMIDAZOISO[5,1-A]QUINOLINES AS FSH RECEPTOR AGONISTS FOR THE TREATMENT OF FERTILITY DISORDERS
申请人:Merck Sharp & Dohme B.V.
公开号:EP2435433B1
公开(公告)日:2013-08-28
US8071587B2
申请人:——
公开号:US8071587B2
公开(公告)日:2011-12-06
A synthesis of dihydroimidazo[5,1-a]isoquinolines using a sequential Ugi–Bischler–Napieralski reaction sequence
作者:W. Michael Seganish、Ana Bercovici、Ginny D. Ho、Hubert J.J. Loozen、Cornelis M. Timmers、Deen Tulshian
DOI:10.1016/j.tetlet.2011.12.050
日期:2012.2
A flexible route to analogues of dihydroimidazo[5,1-a]isoquinolines is described. The synthesis hinges on a sequential Ugi coupling, followed by a Bischler–Napieralski reaction to form the imidazole isoquinoline core. This route facilitates the introduction of a range of substitutions throughout the carbon framework.
描述了制备二氢咪唑并[5,1- a ]异喹啉类似物的灵活途径。合成取决于顺序的Ugi偶联,然后进行Bischler-Napieralski反应以形成咪唑异喹啉核心。该途径有助于在整个碳框架中引入一系列取代基。
(DIHYDRO)IMIDAZOISO[5,1-A]QUINOLINES
申请人:Loozen Hubert Jan Jozef
公开号:US20100324021A1
公开(公告)日:2010-12-23
The invention relates to imidazoiso[5,1-a]quinoline and 5,6-dihydro-imidazoiso[5,1-a]quinoline derivatives according to general Formula I
or a pharmaceutically acceptable salt thereof. The compounds can be used for the treatment of infertility.