反应 #1135831

ord-da8d10456f154bfaadf1d0d11749c3e7

反应方程式

COC(=O)CCCCCCC(=O)Nc1ccc(Br)cc1N
methyl 8-(2-amino-4-bromophenylamino)-8-oxooctanoate
CC(=O)O
acetic acid
COC(=O)CCCCCCc1nc2cc(Br)ccc2[nH]1
methyl 7-(5-bromo-1H-benzimidazol-2-yl)heptanoate
收率 84.3%

溶剂

反应条件

温度
110°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩concentrated
  2. 2
    其他The residue was purified by biotage column chromatography

实验过程

To a solution of methyl 8-(2-amino-4-bromophenylamino)-8-oxooctanoate (140 mg, 0.395 mmol) in toluene was added a drop of acetic acid. The reaction was heated to 110° C. overnight and concentrated. The residue was purified by biotage column chromatography to give methyl 7-(5-bromo-1H-benzimidazol-2-yl)heptanoate (113 mg)

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09381196B2uspto-grants-2016_07