HRID471164

反应详情

EQUATION

反应方程式

HRID 471164 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of (2-isopropylthiazol-4-yl)(1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanone trifluoroacetate (example 22, step b) (0.178 g) in NMP (2 mL) was treated with acetic acid (0.032 mL) and stirred for 5 minutes. A solution of 4-chloro-3-(2-hydroxyethyl)benzaldehyde (example 75, step c) (0.154 g) in NMP (3 mL) was then added, the resulting solution was stirred for 1 hour and was then treated with sodium triacetoxyborohydride (0.181 g) and stirred overnight at room temperature. More sodium triacetoxyborohydride (0.404 g) was added and the mixture was stirred for an additional 6 hours, then poured into saturated sodium bicarbonate and extracted twice with ethyl acetate. The combined extracts were washed three times with water, once with brine, then dried over anhydrous magnesium sulphate and purified by flash chromatography on silica eluted with 1:2:97 triethylamine:methanol:dichloromethane to afford the subtitled compound as a colourless gum. Yield 0.157 g.

WORKUP

后处理

  1. stirringthe resulting solution was stirred for 1 hour
  2. stirringstirred overnight at room temperature
  3. stirringthe mixture was stirred for an additional 6 hours
  4. extractionextracted twice with ethyl acetate
  5. washThe combined extracts were washed three times with water
  6. dry with materialonce with brine, then dried over anhydrous magnesium sulphate
  7. custompurified by flash chromatography on silica
  8. washeluted with 1:2:97 triethylamine