SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4-{3[CIS-HEXAHYDROCYCLOPENT A[CjPYRROL-2( 1 H)-YLjPROPOXYj BENZAMI DE HYDROCHLORI DE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT
申请人:LES LABORATOIRES SERVIER
公开号:US20140155453A1
公开(公告)日:2014-06-05
Medicinal products containing the crystalline form I of the compound of formula (I):
and/or crystalline form I of the associated free base which are useful in the treatment of disorders of the histaminergic system.
Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1H)-yl]proxy}benzamide hydrochloride and pharmaceutical compositions containing it
申请人:Robert Nicolas
公开号:US08664408B2
公开(公告)日:2014-03-04
Industrial synthesis process for, and crystalline form I of, the compound of formula (I):
and also crystalline form I of the associated free base.
Medicinal products containing the same which are useful in the treatment of disorders of the histaminergic system.
Synthesis process, and crystalline form of 4-{3-[cis-hexahydrocyclopenta[c]pyrrol-2(1H)-yl]propoxy} benzamide hydrochloride and pharmaceutical compositions containing it
申请人:Les Laboratoires Servier
公开号:US08952179B2
公开(公告)日:2015-02-10
Industrial synthesis process for the compound of formula (I):
化合物(I)的工业合成过程:
SYNTHESIS PROCESS, AND CRYSTALLINE FORM OF 4- BENZAMIDE HYDROCHLORIDE AND PHARMACEUTICAL COMPOSITIONS CONTAINING IT
申请人:LES LABORATOIRES SERVIER
公开号:US20140100374A1
公开(公告)日:2014-04-10
Industrial synthesis process for the compound of formula (I):
公式(I)的工业合成过程:
Bi-functional complexes and methods for making and using such complexes
申请人:Gouliaev Alex Haahr
公开号:US11225655B2
公开(公告)日:2022-01-18
The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.