METHOXY AND HYDROXY DERIVATIVES OF 3,4-DIHYDRO-3-(DI-NORMAL-PROPYLAMINO)-2H-1-BENZOPYRANS - NEW SYNTHESIS AND DOPAMINERGIC ACTIVITY

被引:16
作者
ALNEIRABEYEH, M
REYNAUD, D
PODONA, T
OU, L
PERDICAKIS, C
COUDERT, G
GUILLAUMET, G
PICHAT, L
GHARIB, A
SARDA, N
机构
[1] UNIV ORLEANS,CHIM BIOORGAN & ANALYT LAB,CNRS,URA 499,BP 6759,F-45067 ORLEANS 2,FRANCE
[2] INST NATL SCI APPL,INSERM,4205,CHIM BIOL LAB,F-69621 VILLEURBANNE,FRANCE
[3] CENS,F-91191 GIF SUR YVETTE,FRANCE
[4] FAC PHARM NANCY,CHIM ORGAN LAB,F-54000 NANCY,FRANCE
关键词
3,4-DIHYDRO-3-AMINO-2H-1-BENZOPYRANS; RACEMIC SYNTHESIS AND RESOLUTION; DOPAMINERGIC RECEPTORS; BRAIN; RAT;
D O I
10.1016/0223-5234(91)90145-D
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The synthesis of methoxy and hydroxy derivatives of 3,4-dihydro-3-(di-n-propylamino)-2H-1-benzopyran from readily available or commercial omicron-hydroxybenzaldehydes is described in six steps. The enantiomers of 8-hydroxy-3,4-dihydro-3-(di-n-propylamino)-2H-1-benzopyran 1b have been resolved. It is shown that the compound (-)-1b is a more selective D-2 agonist, compared to apomorphine.
引用
收藏
页码:497 / 504
页数:8
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