HRID1493281

反应详情

EQUATION

反应方程式

HRID 1493281 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

2-(3-Bromo-2-hydroxypropyl)naphtho[1,8-cd]isothiazole 1,1-dioxide (26.8 g), triethylamine (11 cc) and 4(4-fluorophenyl)piperazine (14.1 g) in toluene (280 cc) are heated at boiling point for 8 hours. The mixture is then cooled to a temperature of about 20° C. and stirring is maintained for 15 hours at this temperature. The precipitate formed is separated by filtration and washed with toluene (2 x 50 cc). The filtrate is evaporated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue obtained is purified by chromatography on a silica column, with ethyl acetate as eluant, and recrystallized from boiling acetonitrile (120 cc). 2-(3[4-(4-Fluorophenyl)-1-piperaz-invl]-2-hydroxypropyl}naphtho[1,8-cd]isothiazole 1,1-dioxide (16.2 g) is obtained, m.p. 130° C.

WORKUP

后处理

  1. customfor 8 hours
  2. temperatureis maintained for 15 hours at this temperature
  3. customThe precipitate formed
  4. customis separated by filtration
  5. washwashed with toluene (2 x 50 cc)
  6. customThe filtrate is evaporated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa)
  7. customThe residue obtained
  8. customis purified by chromatography on a silica column, with ethyl acetate as eluant
  9. customrecrystallized