HRID2175667

反应详情

EQUATION

反应方程式

HRID 2175667 的结构方程式

CONDITIONS

反应条件

温度
150 °C

PROCEDURE

实验过程

To a mixture of (R)-tert-butyl 3-(4-amino-6-cyano-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)pyrrolidine-1-carboxylate (101) (2.0 g, 4.0 mmol) in ethylene glycol/H2O (20 mL/5 mL) was added and NaOH (1.0 g, 25 mmol). The reaction mixture was purged with N2 (2×) before heated at 150° C. overnight. After cooling to r.t., the reaction was diluted with ice-water, neutralized to pH 7 by slow addition of con. HCl. The aqueous layer was washed with DCM, concentrated under vacuum. Part of the residue was purified by preparative HPLC (RP, C18, 10 to 95% acetonitrile in water (0.2% HCOOH)) to give (R)-4-amino-5-(4-phenoxyphenyl)-7-(pyrrolidin-3-yl)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid (127) (60 mg, 4%) as a white solid. LC-MS (ESI): m/z (M+1) 416.0.

WORKUP

后处理

  1. additionwas added
  2. customThe reaction mixture was purged with N2 (2×)
  3. temperatureAfter cooling to r.t.
  4. additionthe reaction was diluted with ice-water
  5. additionneutralized to pH 7 by slow addition of con
  6. washThe aqueous layer was washed with DCM
  7. concentrationconcentrated under vacuum
  8. customPart of the residue was purified by preparative HPLC (RP, C18, 10 to 95% acetonitrile in water (0.2% HCOOH))