Total syntheses of racemic albifloranine and its anti-addictive congeners,including 18-methoxycoronaridine

Citation
Uk. Bandarage et al., Total syntheses of racemic albifloranine and its anti-addictive congeners,including 18-methoxycoronaridine, TETRAHEDRON, 55(31), 1999, pp. 9405-9424
Citations number
31
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
55
Issue
31
Year of publication
1999
Pages
9405 - 9424
Database
ISI
SICI code
0040-4020(19990730)55:31<9405:TSORAA>2.0.ZU;2-3
Abstract
Condensation of methyl 3-benzyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5 -carboxylate (12) with 4-(1,3-dioxolan-2-yl)-6-benzylaxyhexanal (11a) provi ded the tetracyclic intermediates methyl (3aSR,4RS,11bRS)-3-benzyl-2,3,3a,4 ,5,7-hexahydro-4-[2-zeta-(1,3-dioxalan-2-yl)-4-benzyloxy)-1-butyl]-1H-pyrro lo[2,3-d]carbazole-6-carboxylates (14a,15a), which were further elaborated to afford racemic albifloranine (3). The first total synthesis of albiflora nine was completed in 13 steps, with an overall 7% yield. Ester and ether d erivatives of albifloranine were synthesized for evaluation as anti-addicti ve agents. Among these, 18-methoxycoronaridine (20b) stands out as a nontox ic agent that significantly reduces demand for morphine, cocaine, nicotine and alcohol in rats. (C) 1999 Elsevier Science Ltd. All rights reserved.