HRID1777981

反应详情

EQUATION

反应方程式

HRID 1777981 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A mixture of 2-(dimethoxymethyl)-5,6,7,8-tetrahydro-1,8-naphthyridine-3-carbaldehyde (intermediate 41, 156 mg, 0.660 mmol), (R)-phenyl(5-cyano-4-((1-methoxypropan-2-yl)oxy)pyridin-2-yl)carbamate (intermediate 145, 281 mg, 0.858 mmol) and DMAP (121 mg, 0.990 mmol) in DMF (3 ml) was heated for 1 h at 90° C. The cooled reaction mixture was partitioned between EtOAc and saturated aqueous NaHCO3 solution, extracted 2× with EtOAc, the organic layers dried over Na2SO4 and evaporated. The residue was applied to a 40 g RediSep® column and purified by normal phase chromatography, eluting with hetane and then a gradient from DCM to 10% MeOH in DCM. Product containing fractions were combined and evaporated to give the title compound. (UPLC-MS 6) tR 1.20; ESI-MS 470.2 [M+H]+.

WORKUP

后处理

  1. customThe cooled reaction mixture
  2. customwas partitioned between EtOAc and saturated aqueous NaHCO3 solution
  3. extractionextracted 2× with EtOAc
  4. dry with materialthe organic layers dried over Na2SO4
  5. customevaporated
  6. custompurified by normal phase chromatography
  7. washeluting with hetane
  8. additionProduct containing fractions
  9. customevaporated