反应 #595376

ord-8294b3517441414c81b59b42493ccab1

反应方程式

Brc1n[nH]c2ccccc12
3-bromo-1H-indazole
CCN(CC)CC
triethylamine
N#Cc1ccccc1S(=O)(=O)Cl
2-cyanobenzene-1-sulfonyl chloride
N#Cc1ccccc1S(=O)(=O)n1nc(Br)c2ccccc21
3-bromo-1-(2-cyanophenylsulfonyl)-1H-indazole
收率 97.4%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩After completion the reaction mixture was concentrated under reduced pressure
  2. 2
    其他the product was purified on SiO2 using 0% to 50% ethyl acetate in heptane as the eluent

实验过程

To a solution of 3-bromo-1H-indazole (200 mg, 1.02 mmol) in 2 ml CH2Cl2 was added triethylamine (308 mg, 3.05 mmol) and 2-cyanobenzene-1-sulfonyl chloride (205 mg, 1.02 mmol). The reaction mixture was stirred overnight at room temperature. After completion the reaction mixture was concentrated under reduced pressure and the product was purified on SiO2 using 0% to 50% ethyl acetate in heptane as the eluent to give 3-bromo-1-(2-cyanophenylsulfonyl)-1H-indazole (360 mg) as a yellow solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09095583B2uspto-grants-2015_08