HRID1657668

反应详情

EQUATION

反应方程式

HRID 1657668 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
5 °C

PROCEDURE

实验过程

1-Hydroxy-6-chloro-2-(trifluoromethyl)-1H-imidazo-(4,5-b)pyridine (5 grams) in 15 milliliters of pyridine was cooled to 5°C. with stirring and methylsulfonyl chloride (5 milliliters) was added in 1-milliliter portions, maintaining the temperature at about 5°C. After the addition was completed, the reaction mixture was stirred for 2 hours at 5°-10°C., then poured into 30 grams of ice and 20 milliliters of concentrated hydrochloric acid. The desired 1-(methylsulfonyloxy)-6-chloro-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine product precipitated and was separated by filtration and washed with water. The washed product was taken up in diethyl ether with a trace of acetone, dried over magnesium sulfate and the solvent evaporated under vacuum. The product so obtained melted at 136.7°C.

WORKUP

后处理

  1. additionAfter the addition
  2. stirringthe reaction mixture was stirred for 2 hours at 5°-10°C.
  3. customThe desired 1-(methylsulfonyloxy)-6-chloro-2-(trifluoromethyl)-1H-imidazo(4,5-b)pyridine product precipitated
  4. customwas separated by filtration
  5. washwashed with water
  6. dry with materialdried over magnesium sulfate
  7. customthe solvent evaporated under vacuum