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WJPR Citation
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| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
AN IMPROVED AND CONVENIENT ROUTE FOR THE SYNTHESIS OF 5-METHYL-1H-TETRAZOL-1-YL SUBSTITUTED BENZENAMINES
Suresh G. Vedpathak*, R. G. Momle, Gopal K. Kakade and Vilas S. Ingle
Abstract An improved and convenient route for the synthesis of a series of 5-methyl-1H-tetrazol-1-yl substituted benzenamines have been reportedvia multi-step reactions from nitroanilines. 1, 5-Disubstituted tetrazolecontaining nitrobenzenes 3 have neen synthesized fromnitroacetanilides 2 by reacting with sodium azide in the presence oftitanium tetrachloride as a catalyst. The reduction of 1, 5-disubstitutedtetrazole containing nitrobenzenes 3 which on using NaBH4 gives 5-methyl-1H-tetrazol-1-yl substituted benzenamines 4 in good toexcellent yields. Keywords: Benzenamines, Reduction, Tetrazoles, Titanium tetrachloride. [Full Text Article] [Download Certificate] |
