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由内烯烃和端烯烃脂肪酸简便一锅法合成N-酰基-1H-1,2,3-苯并三唑及其抗菌筛选

Facile one-pot synthesis of N-acyl-1H-1,2,3-benzotriazoles from internal and terminal olefinic fatty acids and their antimicrobial screening.

作者信息

Rauf Abdul, Gangal Saloni

机构信息

Department of Chemistry, Aligarh Muslim University, Aligarh, India.

出版信息

J Oleo Sci. 2008;57(8):453-7. doi: 10.5650/jos.57.453.

DOI:10.5650/jos.57.453
PMID:18622129
Abstract

N-acyl-1H-1,2,3-benzotriazoles were prepared in good yields by the reaction of benzotriazole and thionyl chloride with olefinic fatty acids under mild reaction conditions. The new compounds 1-(undec-10-enoyl)-1H-1,2,3-benzotriazole (5a),1-[(Z)-octadec-9-enoyl]-1H-1,2,3-benzotriazole (5b), 1-[(9Z,12R)-12-hydroxyoctadec-9-enoyl]-1H-1,2,3-benzotriazole (5c), 1-[(9R,12Z)-9-hydroxyoctadec-12-enoyl]-1H-1,2,3-benzotriazole (5d) formed were characterized on the basis of elemental analysis and spectral data. All the newly synthesized compounds (5a-5d) were screened for their antimicrobial activity and showed good antifungal activity.

摘要

在温和的反应条件下,通过苯并三唑、亚硫酰氯与烯属脂肪酸反应,以良好的产率制备了N-酰基-1H-1,2,3-苯并三唑。基于元素分析和光谱数据对新形成的化合物1-(十一碳-10-烯酰基)-1H-1,2,3-苯并三唑(5a)、1-[(Z)-十八碳-9-烯酰基]-1H-1,2,3-苯并三唑(5b)、1-[(9Z,12R)-12-羟基十八碳-9-烯酰基]-1H-1,2,3-苯并三唑(5c)、1-[(9R,12Z)-9-羟基十八碳-12-烯酰基]-1H-1,2,3-苯并三唑(5d)进行了表征。对所有新合成的化合物(5a - 5d)进行了抗菌活性筛选,结果显示它们具有良好的抗真菌活性。

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