反应 #2320151

ord-59258f021c294dd98808f01ec494dca2

反应方程式

O=CNC(=O)Cc1ccccc1
N-Formylphenylacetamide
Cl.NNc1cccc(Cl)c1Cl
2,3-dichlorophenylhydrazine hydrochloride
Clc1cccc(-n2ncnc2Cc2ccccc2)c1Cl
title compound
Clc1cccc(-n2ncnc2Cc2ccccc2)c1Cl
5-benzyl-1-(2,3-dichlorophenyl)-1H-1,2,4-triazole

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度refluxed under a nitrogen atmosphere for 1 hour
  2. 2
    浓缩concentrated under reduced pressure at 60° C
  3. 3
    其他The residue was purified by flash chromatography
  4. 4
    洗涤eluting with hexanes/ethyl acetate (6/1)

实验过程

N-Formylphenylacetamide (Finkbeiner J. Org. Chem. 1965, 30; 2861) (200 mg, 1.22 mmol) and 2,3-dichlorophenylhydrazine hydrochloride (314 mg, 1.47 mmol) were combined in glacial acetic acid (8 mL) and refluxed under a nitrogen atmosphere for 1 hour and then concentrated under reduced pressure at 60° C. The residue was purified by flash chromatography eluting with hexanes/ethyl acetate (6/1) to provide the title compound. MS (ESI+) m/z 305 (M+1H)+; 1H NMR (300 MHz, DMSO-d6) δ ppm 4.02 (s, 2H) 6.97-7.02 (m, 2H) 7.16-7.25 (m, 3H) 7.52-7.58 (m, 2H) 7.88 (dd, J=6.8, 3.1 Hz, 1H) 8.16 9s, 1 H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07709469B2uspto-grants-2010_05