HRID1491921

反应详情

EQUATION

反应方程式

HRID 1491921 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
75 °C

PROCEDURE

实验过程

A mixture of 3-(4-bromobutyl)-5,5-dimethyl-4-thiazolidinone (4.00 g), 1-(2-methylphenyl)-piperazine (3.87 g), K2CO3 (8.31 g), NaI (290 mg) and acetonitrile (175 ml) was heated at 75° C. (bath temperature) under nitrogen. After 16 hours, TLC analysis (silica gel, 5% MeOH/CH2Cl2) showed absence of the starting bromide and presence of a major product, Rf =0.24. The reaction mixture was cooled to room temperature, ethyl acetate (150 ml) was added, and the mixture filtered. The filtrate was concentrated in vacuo to an oil which was dissolved into ethyl acetate causing a solid to precipitate. The mixture was filtered and the filtrate concentrated in vacuo to 6.35 g of an oil. The oil was chromatographed (5% MeOH/CH2CI2, one silica gel column) to obtain 4.91 g of a solid. The solid was dissolved in diethylether (550 ml), the solution filtered m remove a trace of insoluble material, and the filtrate acidified to pH=1 with a HCl/diethylether solution. The resulting salt was collected and dried to give 4.83 g of powder. The powder was recrystallized from ethanol/ethyl acetate to yield 2.14 g of crystals. m.p. 230°-235° C.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationthe mixture filtered
  3. concentrationThe filtrate was concentrated in vacuo to an oil which
  4. dissolutionwas dissolved into ethyl acetate causing a solid
  5. customto precipitate
  6. filtrationThe mixture was filtered
  7. concentrationthe filtrate concentrated in vacuo to 6.35 g of an oil
  8. customThe oil was chromatographed (5% MeOH/CH2CI2, one silica gel column)