[EN] 7,11-METHANOCYCLOOCTA [B] QUINOLINE DERIVATIVE AS HIGHLY FUNCTIONALIZABLE ACETYLCHOLINESTERASE INHIBITORS [FR] DÉRIVÉ DE 7,11-METHANOCYCLOOCTA [B] QUINOLINE UTILISÉ COMME INHIBITEURS DE L'ACÉTYLCHOLINESTÉRASE POUVANT ÊTRE HAUTEMENT FONCTIONNALISÉS
7,11-Methanocycloocta[b]quinoline derivative as highly functionalizable acetylcholinesterase inhibitors
申请人:Universite de Rouen
公开号:EP2377853A1
公开(公告)日:2011-10-19
The present invention concerns new highly functionalizable Huprine derivatives of formula I:
a method for preparing such compounds and their use for treating neurological diseases in which the level of acetylcholine is affected such as Alzheimer's disease; their use for affinity chromatography as well as their use as enantioselective catalyst.
7,11-methanocycloocta [B] quinoline derivative as highly functionalizable acetylcholinesterase inhibitors
申请人:Ronco Cyril
公开号:US09040506B2
公开(公告)日:2015-05-26
New highly functionalizable Huprine derivatives of formula I:
and
a method for preparing such compounds and their use for treating neurological diseases in which the level of acetylcholine is affected such as Alzheimer's disease.
7,11-METHANOCYCLOOCTA [B] QUINOLINE DERIVATIVE AS HIGHLY FUNCTIONALIZABLE ACETYLCHOLINESTERASE INHIBITORS
申请人:UNIVERSITE DE ROUEN
公开号:US20150197735A1
公开(公告)日:2015-07-16
New highly functionalizable Huprine derivatives of formula I:
and
a method for preparing such compounds and their use for treating neurological diseases in which the level of acetylcholine is affected such as Alzheimer's disease.
7,11-methanocycloocta [b] quinoline derivative as highly functionalizable acetylcholinesterase inhibitors
申请人:UNIVERSITE DE ROUEN
公开号:US09290750B2
公开(公告)日:2016-03-22
New highly functionalizable Huprine derivatives of formula I:
and
a method for preparing such compounds and their use for treating neurological diseases in which the level of acetylcholine is affected such as Alzheimer's disease.
Improved synthetic pathway for the derivatization of huprine scaffold
作者:Cyril Ronco、Ludovic Jean、Pierre-Yves Renard
DOI:10.1016/j.tet.2010.07.021
日期:2010.9
In the search of new huprine-like acetylcholinesterase binders, we have developed an improved, shorter, and high-scalable synthetic pathway for the huprine synthesis based on a Reformatsky reaction–one-pot fragmentation/Friedländer condensation sequence. An extension for the one-pot synthesis of huprine-like 4-chloroquinolines is also presented. This modified route is particularly interesting as it