HRID1427476

反应详情

EQUATION

反应方程式

HRID 1427476 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

A mixture of (S)-methyl 6-[(3-methyl-1-{4-[5-(trifluoromethyl)pyridin-2-yl]phenyl}butyl)amino]nicotinate (53.0 g, 119.5 mmol) was dissolved in methanol (239 ml) and tetrahydrofuran (120 ml) and treated with aqueous lithium hydroxide (120 ml, 239 mmol, 2.0M). An additional aliquot of methanol was added to homogenize the mixture (110 ml, ˜2 ml/g). The reaction was heated to 50° C. for 12 h. The reaction was concentrated in vacuo, and the crude residue was diluted with water (500 ml). The solution was vigorously stirred and slowly acidified with aqueous 1.0M hydrochloric acid (240 ml, to approximately pH 5.0). The precipitated solid was collected by filtration and the remaining solid was dissolved with ethyl acetate and transferred into a separate flask. The crude solid was dried in vacuo and used directly for further transformations.

WORKUP

后处理

  1. concentrationThe reaction was concentrated in vacuo
  2. additionthe crude residue was diluted with water (500 ml)
  3. stirringThe solution was vigorously stirred
  4. filtrationThe precipitated solid was collected by filtration
  5. dissolutionthe remaining solid was dissolved with ethyl acetate
  6. customtransferred into a separate flask
  7. customThe crude solid was dried in vacuo