Novel bronchodilatory quinazolines and quinoxalines: Synthesis and biological evaluation
摘要:
A series of heterocyclic derivatives analogous to (-)vasicinone, in which the vasicinone C-ring was replaced with alkyl chain terminated by tertiary amine was prepared. N3, C4-O, C4-S or C4-N were used as the sites of attachment. The 4-[3-(1-piperidyl)propylsulfanyl]derivatives displayed bronchodilatory effect at low micromolar concentrations on isolated rat trachea, and low toxicity both on Balb/c 3T3 mouse fibroblast cells and in mice. (C) 2014 Elsevier Masson SAS. All rights reserved.
Synthesis of 3-Substituted and 2,3-Disubstituted Quinazolinones via Cu-Catalyzed Aryl Amidation
作者:Lanting Xu、Yongwen Jiang、Dawei Ma
DOI:10.1021/ol300084v
日期:2012.2.17
Cul/4-hydroxy-L-proline catalyzed coupling of N-substituted o-bromobenzamides with formamide takes place at 80 degrees C, affording 3-substituted quinazolinones directly. Under these conditions other amides that were tested only provided simple coupling products, which can be converted into 2,3-disubstituted quinazolinones via HMDS/ZnCl2 mediated condensative cyclization.
Sen,A.B.; Singh,S.B., Journal of the Indian Chemical Society, 1965, vol. 42, p. 409 - 411
作者:Sen,A.B.、Singh,S.B.
DOI:——
日期:——
Novel bronchodilatory quinazolines and quinoxalines: Synthesis and biological evaluation
作者:Marcel Špulák、Jana Pourová、Marie Vopršálová、Jiří Mikušek、Jiří Kuneš、Jan Vacek、Mukund Ghavre、Nicholas Gathergood、Milan Pour
DOI:10.1016/j.ejmech.2013.12.024
日期:2014.3
A series of heterocyclic derivatives analogous to (-)vasicinone, in which the vasicinone C-ring was replaced with alkyl chain terminated by tertiary amine was prepared. N3, C4-O, C4-S or C4-N were used as the sites of attachment. The 4-[3-(1-piperidyl)propylsulfanyl]derivatives displayed bronchodilatory effect at low micromolar concentrations on isolated rat trachea, and low toxicity both on Balb/c 3T3 mouse fibroblast cells and in mice. (C) 2014 Elsevier Masson SAS. All rights reserved.