HRID1445192

反应详情

EQUATION

反应方程式

HRID 1445192 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

A mixture of 102 mg (0.340 mmol) 1-(3-bromo-4-nitro-phenyl)-4-methyl-piperazine (as prepared in Example 9, step (a)), 59.7 mg (0.474 mmol) cyclohexen-1-ylboronic acid, 43.8 mg (0.0379 mmol) of tetrakis(triphenylphosphine)palladium (0) under Ar was treated with 206 μL (0.412 mmol) of 2.0 M degassed aq Na2CO3, 0.6 mL degassed anh toluene and 0.2 mL degassed anh EtOH and the mixture was heated at 100° C. for 21 h. After cooling to RT, the mixture was poured into EtOAc (10 mL), washed with brine (10 mL), dried (Na2SO4) and concentrated in vacuo. Chromatography on a 5-g silica SPE column with 1-3% EtOH in dichloromethane afforded 126 mg of the title compound (74% purity by RP-HPLC (C18 column) as a mixture with triphenylphosphine) as a yellow oil that was used in the following reaction without further purification. Mass spectrum (ESI, m/z): Calcd. for C17H23N3O3, 302.2 (M+H), found 302.2.

WORKUP

后处理

  1. additionwas treated with 206 μL (0.412 mmol) of 2.0 M
  2. customdegassed aq Na2CO3, 0.6 mL
  3. customdegassed anh toluene and 0.2 mL
  4. customdegassed anh EtOH
  5. temperatureAfter cooling to RT
  6. additionthe mixture was poured into EtOAc (10 mL)
  7. washwashed with brine (10 mL)
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated in vacuo