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Regioselective N1‐methylation of 1H‐tetrazoles with methyl 2,2,2‐trichloroacetimidate
Journal of Heterocyclic Chemistry ( IF 2.4 ) Pub Date : 2024-05-10 , DOI: 10.1002/jhet.4824 Sudhakar Reddy Baddam 1 , Sudhakar Kalagara 2 , Srinivas Ganta 3 , Venkata Suresh Ponnuru 4 , Balaraju Vudari 5 , Seshadri Nalla 6
Journal of Heterocyclic Chemistry ( IF 2.4 ) Pub Date : 2024-05-10 , DOI: 10.1002/jhet.4824 Sudhakar Reddy Baddam 1 , Sudhakar Kalagara 2 , Srinivas Ganta 3 , Venkata Suresh Ponnuru 4 , Balaraju Vudari 5 , Seshadri Nalla 6
Affiliation
An efficient, mild, and regioselective synthesis of substituted 1‐methyl‐1H ‐tetrazole using methyl 2,2,2‐trichloroacetimidate is described. The substrate scope of the methodology has been established with wide variety of tetrazoles. N 1‐Methylated tetrazoles were synthesized with high yields (85%–97%).
中文翻译:
1H-四唑与 2,2,2-三氯乙酰亚氨酸甲酯的区域选择性 N1-甲基化
描述了使用 2,2,2-三氯乙酰亚氨酸甲酯高效、温和且区域选择性合成取代的 1-甲基-1H-四唑。该方法的底物范围已确定为多种四唑。 N1-甲基化四唑的合成收率很高(85%–97%)。
更新日期:2024-05-10
中文翻译:
1H-四唑与 2,2,2-三氯乙酰亚氨酸甲酯的区域选择性 N1-甲基化
描述了使用 2,2,2-三氯乙酰亚氨酸甲酯高效、温和且区域选择性合成取代的 1-甲基-1H-四唑。该方法的底物范围已确定为多种四唑。 N1-甲基化四唑的合成收率很高(85%–97%)。