تفاعل #640521

ord-77896f8fc5af43b394fa71834f395fe8

معادلة التفاعل

Nc1nonc1-c1nc2ccccc2[nH]1
4-(1H-benzimidazol-2-yl)-furazan-3-ylamine
CO
methanol
C=CC#N
acrylonitrile
N#CCCNc1nonc1-c1nc2ccccc2[nH]1
title compound
N#CCCNc1nonc1-c1nc2ccccc2[nH]1
4-(1H-Benzimidazol-2-yl)-furazan-3-yl-N-(2-cyanoethyl)-amine

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىEvaporation of the solvent under reduced pressure
  2. 2
    أخرىpartitioning of the resulting residue between water and ethyl acetate
  3. 3
    تجفيفby drying of the organic solution over sodium sulphate

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE042890E1uspto-grants-2011_11