HRID226344

反应详情

EQUATION

反应方程式

HRID 226344 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of ethyl (2E)-3-(6-{(tert-butoxycarbonyl)[(3R)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate dihydrochloride (3.0 g) in 1,2-dichloroethane (30 mL) was added diisopropylethylamine (2.41 mL) and 3-fluorobenzaldehyde (857 mg), and the mixture was stirred at room temperature for 5 minutes. To the mixture was added sodium triacetoxyborohydride (3.1 g) and stirred for 3 hours, and resulting mixture was poured into sat NH4Cl aq solution, and extracted with AcOEt. The organic layer was washed with sat NH4Cl aq solution, water, and brine, and dried over Na2SO4. The solvent was removed in vacuo and the residual oil was purified by silica gel column chromatography eluted with AcOEt and hexane (1:1) to give ethyl (2E)-3-(6-{(tert-butoxycarbonyl)[(3R)-1-(2-fluorobenzyl)-3-pyrrolidinyl]amino}-3-pyridyl)acrylate (2.40 g) as colorless oil.

WORKUP

后处理

  1. stirringstirred for 3 hours
  2. customresulting mixture
  3. additionwas poured
  4. extractionextracted with AcOEt
  5. washThe organic layer was washed with sat NH4Cl aq solution, water, and brine
  6. dry with materialdried over Na2SO4
  7. customThe solvent was removed in vacuo
  8. customthe residual oil was purified by silica gel column chromatography
  9. washeluted with AcOEt and hexane (1:1)