HRID2227672

反应详情

EQUATION

反应方程式

HRID 2227672 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 1.54 g (3.85 mmol) of 2-methoxymethylthiazolo[5,4-b]pyridin-6-yl-carboxylic acid-N-phenyl-N-(2-ethoxycarbonylethyl)amide and 4.3 ml (4.3 mmol) of a 1 molar solution of boron tribromide in methylene chloride was dissolved in a further 30 ml of methylene chloride and stirred for 5 hours at room temperature. Then the mixture was washed with 40 ml of saturated sodium hydrogen carbonate solution, the organic phase was dried with sodium sulfate, and the solvent was distilled off. The crude product (1.9 g) was taken up in 15.0 ml of N,N-diisopropylethylamine, mixed with 0.50 g (4.2 mmol) of 4-aminobenzonitrile, and heated to boiling for one hour. Then the solvent was distilled off in vacuo, the crude product was taken up in 100 ml of methylene chloride, the organic phase was washed with 100 ml of water, and dried with sodium sulfate. After the solvent had been removed in vacuo, the crude product obtained was purified by flash chromatography (silica gel; ethyl acetate/petroleum ether=35:65 to 1:1) and evaporated down again in vacuo.

WORKUP

后处理

  1. washThen the mixture was washed with 40 ml of saturated sodium hydrogen carbonate solution
  2. dry with materialthe organic phase was dried with sodium sulfate
  3. distillationthe solvent was distilled off
  4. temperatureheated
  5. waitto boiling for one hour
  6. distillationThen the solvent was distilled off in vacuo
  7. washthe organic phase was washed with 100 ml of water
  8. dry with materialdried with sodium sulfate
  9. customAfter the solvent had been removed in vacuo