SYNTHESIS OF 6,7-DIHYDRO-8-(4-METHYL-1-PIPERAZINYL)-[1]BENZOXEPINO[4,5-C]QUINOLINE AS POTENTIAL 5-HT3 RECEPTOR-LIGAND

被引:6
作者
ANZINI, M
CAPPELLI, A
VOMERO, S
机构
[1] Dipartimento Farmaco Chimico Tecnologico - Università di Siena - Banchi di Sotto
关键词
D O I
10.3987/COM-92-6276
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two synthetic routes to the achievement of the title compound are described. The [1]benzoxepino[4,5-c]quinoline nucleus was prepared by nucleophilic aromatic fluoride displacement-cyclization and functionalized with N-methylpiperazine moiety. Alternatively the oxepino ring closure is shifted as the final step. An oxepine ring cleavage occurred in compounds (9) and (3); a mechanistical interpretation is proposed.
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页码:1065 / 1074
页数:10
相关论文
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[1]   SYNTHESIS OF 6-(4-METHYL-1-PIPERAZINYL)-7H-INDENO[2,1-C]QUINOLINE DERIVATIVES AS POTENTIAL 5-HT RECEPTOR LIGANDS [J].
ANZINI, M ;
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JOURNAL OF HETEROCYCLIC CHEMISTRY, 1991, 28 (07) :1809-1812
[2]   NUCLEOPHILIC DISPLACEMENT OF AROMATIC FLUORINE .4. QUINOLINOQUINOLINES AND BENZOCHROMENOQUINOLINES [J].
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