HRID417879

反应详情

EQUATION

反应方程式

HRID 417879 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

5

PROCEDURE

实验过程

A solution of 4-[2-Amino-4-chloro-7-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethyl)-7H-pyrrolo [2,3-d]pyrimidin-5-yl]-but-3-yn-1-ol (see example 2) (51.7 mg), N-Boc alanine (53.3 mg), DMAP (33.7 mg), and EDCI (54.9 mg) in anhyrous DMA (4 mL) was stirred at rt overnight. Work-up (EtOAc; H2O) gave the crude Boc-protected intermediate. A solution of this intermediate (40 mg) in DCM (1.0 (mL) was treated with TFA (0.2 mL) at rt for 5 min, and evaporated. The material was dissolved in MeOH (1 ml) and water (10 mL), and washed with Et2O (10 mL). The organic layer was discarded. The aqueous layer was brought to pH>7 with sat. aq. NaHCO3 and back-extracted with DCM. The title compound was isolates as a solid. HPLC Rt=4.37 min.

WORKUP

后处理

  1. customgave the crude Boc-
  2. customevaporated
  3. dissolutionThe material was dissolved in MeOH (1 ml)
  4. washwater (10 mL), and washed with Et2O (10 mL)
  5. extractionback-extracted with DCM