HRID1071229

反应详情

EQUATION

反应方程式

HRID 1071229 反应方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

1.2 g of ethyl 4-[3-(3-chloro-6-methoxy-quinolin-4-yl)propyl]piperidine-4-carboxylate, 0.51 g of potassium carbonate and 0.61 g of potassium iodide were added, at a temperature in the region of 20° C., with stirring and under an inert atmosphere, to a solution of 0.607 g of (2-chloroethylthio)cyclopentane in 50 cm3 of acetonitrile. After heating for 20 hours at a temperature in the region of 80° C., the reaction mixture was cooled to about 20° C., filtered and concentrated under reduced pressure (1 kPa) at a temperature in the region of 50° C. The residue obtained was purified by chromatography under a nitrogen pressure of 100 kPa, on a column of silica gel (particle size 40-60μ; diameter 3.5 cm), eluting with a mixture of dichloromethane/methanol (98/2 by volume) and collecting 35-cm3 fractions. Fractions 25 to 31 were combined and then concentrated as above. 0.9 g of ethyl 4-[3-(3-chloro-6-methoxyquinolin-4-yl)propyl]-1-[2-(cyclopentylthio)ethyl]piperidine-4-carboxylate was obtained.

WORKUP

后处理

  1. temperaturethe reaction mixture was cooled to about 20° C.
  2. filtrationfiltered
  3. concentrationconcentrated under reduced pressure (1 kPa) at a temperature in the region of 50° C
  4. customThe residue obtained
  5. customwas purified by chromatography under a nitrogen pressure of 100 kPa
  6. washon a column of silica gel (particle size 40-60μ; diameter 3.5 cm), eluting with a mixture of dichloromethane/methanol (98/2 by volume)
  7. customcollecting 35-cm3 fractions
  8. concentrationconcentrated as above