HRID633341

反应详情

EQUATION

反应方程式

HRID 633341 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of (±)-octahydro-5,5-dimethylindolizin-7-amine (0.65 g, 3.9 mmol) in MeOH (10 ml) was added to a stirred solution of 2,4-dichloropyrimidine-5-carboxamide (0.75 g, 3.9 mmol; prepared according to the procedure set forth in US patent application publication US20110130415, page 41) in MeOH (30 ml) and H2O (4 ml) at 0° C. under nitrogen. After complete addition, the mixture was slowly warmed to room temperature and stirred at room temperature overnight. The mixture was then concentrated in vacuo and the residue partitioned between EtOAc (150 ml) and 1N NaOH (100 ml). The aqueous layer was extracted with EtOAc (1×100 ml) and the combined organic extracts were dried (Na2SO4), filtered and the solvent removed in vacuo. The residue was dry-loaded on to basic alumina (Brockmann grade IV) and then purified by column chromatography on basic alumina (Brockmann grade IV) using CH2Cl2/MeOH (1:0 to 95:5) as eluent to give the product (550 mg).

WORKUP

后处理

  1. customprepared
  2. customat 0° C.
  3. additionAfter complete addition
  4. concentrationThe mixture was then concentrated in vacuo
  5. customthe residue partitioned between EtOAc (150 ml) and 1N NaOH (100 ml)
  6. extractionThe aqueous layer was extracted with EtOAc (1×100 ml)
  7. dry with materialthe combined organic extracts were dried (Na2SO4)
  8. filtrationfiltered
  9. customthe solvent removed in vacuo
  10. custompurified by column chromatography on basic alumina (Brockmann grade IV)