HRID11582

反应详情

EQUATION

反应方程式

HRID 11582 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
35 °C

PROCEDURE

实验过程

A mixture of (S)-1-carboxymethyl-3-(5-chloroindole-2-carbonylamino)-3,4-dihydrocarbostyril (Example 10) (6 mg) in 1.0 M borane in tetrahydrofuran solution (2 mL) under argon was stirred at 35° C. for 3 h. After cooling to room temperature, 1.0 M aqueous hydrochloric acid (10 mL) and ethyl acetate (10 mL) were added. This mixture was stirred for 3 h before the layers were separated. The organic phase was washed with water (10 mL three times) and evaporated under vacuum. The residue was chromatographed on reverse phase preparative HPLC to isolate the title compound (1.1 mg) and the over-reduction product (S)-1-(2-hydroxyethyl)-3-(5-chloroindole-2-carbonylamino)-1,2,3,4-tetrahydroquinoline (0.9 mg). Title compound HPLC/MS [M+H]+, 384.

WORKUP

后处理

  1. temperatureAfter cooling to room temperature
  2. stirringThis mixture was stirred for 3 h before the layers
  3. customwere separated
  4. washThe organic phase was washed with water (10 mL three times)
  5. customevaporated under vacuum
  6. customThe residue was chromatographed on reverse phase preparative HPLC