Synthesis of 5-organostibano-1H-1,2,3-triazoles by Cu-catalyzed azide-alkyne cycloaddition and their application in the acyl-induced deantimonation for the preparation of fully substituted 5-acy1-1,2,3triazoles

被引:13
|
作者
Yamada, Mizuki [1 ]
Matsumura, Mio [1 ]
Murata, Yuki [1 ]
Kawahata, Masatoshi [2 ]
Saito, Kohki [1 ]
Kakusawa, Naoki [3 ]
Yamaguchi, Kentaro [2 ]
Yasuike, Shuji [1 ]
机构
[1] Aichi Gakuin Univ, Sch Pharmaceut Sci, Chikusa Ku, 1-100 Kusumoto Cho, Nagoya, Aichi 4648650, Japan
[2] Tokushima Bunri Univ, Pharmaceut Sci, Kagawa Campus,1314-1 Shido, Sanuki, Kagawa 7692193, Japan
[3] Hokuriku Univ, Fac Pharmaceut Sci, Ho 3 Kanagawa Machi, Kanazawa, Ishikawa 9201181, Japan
关键词
Ethynylstibane; Cu-catalyzed azide-alkyne cycloaddition; Antimony; Acyl-induced deantimonation; Acylation; 1,2,3-Triazole; CROSS-COUPLING REACTION; CLICK CHEMISTRY; COPPER(I)-CATALYZED CYCLOADDITION; ORGANIC AZIDES; TRANSMETALLATING AGENT; TRIARYLSTIBINES; KETONES; LIGAND; ORGANOANTIMONY(III); CYTOTOXICITY;
D O I
10.1016/j.tet.2017.03.046
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The Cu-catalyzed azide-alkyne cycloaddition by the reaction of various ethynylstibanes with benzylazide in the presence of CuBr (5 mol%) under aerobic conditions led to the formation of trisubstituted 5organostibano-1H-1,2,3-triazoles. Further, the acyl-induced deantimonation of 5-stibanotriazoles with acyl chlorides in the presence of N,N-dimethyl-4-aminopyridine and triethylamine afforded the corresponding trisubstituted 5-acyltriazoles in moderate-to-good yields. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2614 / 2622
页数:9
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