HRID575114

反应详情

EQUATION

反应方程式

HRID 575114 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

A mixture of 9-Bromo-4,4-difluoro-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester as a yellow solid (166.5 mg, 0.443 mmol), 2-methyl-3-butyn-2-ol (298 mg, 3.544 mmol), Pd(OAc)2 (10 mg, 0.0443 mmol), CuI (17 mg, 0.0886 mmol) and PPh3 (35 mg, 0.1329 mmol) in Et3N (20 mL) was degassed with N2, and the mixture was stirred at 80° C. overnight. The reaction mixture was cooled to room temperature, concentrated and purified by flash column chromatography (silica gel, EtOAc in hexane from 0 to 40%) to give 4,4-Difluoro-9-(3-hydroxy-3-methyl-but-1-ynyl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid methyl ester as a yellow solid (86 mg, 51%). LC-MS (ESI & APCI): 380.4 (M+1).

WORKUP

后处理

  1. customwas degassed with N2
  2. temperatureThe reaction mixture was cooled to room temperature
  3. concentrationconcentrated
  4. custompurified by flash column chromatography (silica gel, EtOAc in hexane from 0 to 40%)