反应 #640521
ord-77896f8fc5af43b394fa71834f395fe8
反应方程式
4-(1H-benzimidazol-2-yl)-furazan-3-ylamine
methanol
acrylonitrile
→
title compound
4-(1H-Benzimidazol-2-yl)-furazan-3-yl-N-(2-cyanoethyl)-amine
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他Evaporation of the solvent under reduced pressure
- 2其他partitioning of the resulting residue between water and ethyl acetate
- 3干燥by drying of the organic solution over sodium sulphate
实验过程
To a solution of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.10 g, 0.497 mmol) in pyridine (5 ml) sodium in methanol (0.02 g, 0.86 mmol in 1 ml) and acrylonitrile (0.03 g, 0.39 mmol) are added sequentially at 0° C. The mixture is stirred over night. Evaporation of the solvent under reduced pressure and partitioning of the resulting residue between water and ethyl acetate followed by drying of the organic solution over sodium sulphate gives the title compound in pure form. 1H-NMR (400 MHz, d6-DMSO): 13.7 (s, 1H); 7.82 (d, 1H); 7.60 (d, 1H); 7.36 (m, 2H); 7.20 (t, 1H); 3.67 (q, 2H); 2.94 (t, 2H).