HRID1976829

反应详情

EQUATION

反应方程式

HRID 1976829 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

A mixture of 380 g of xylene (mixture of isomers), 110 g of ethyl N,N-dimethylaminoacrylate and 77.4 g of triethylamine was initially charged, and 160 g of 2,4-dichloro-5-fluorobenzoyl chloride were added dropwise at 70° C. over a period of 60 minutes. The mixture was subsequently stirred at 70° C. for 2 hours and cooled to room temperature. At room temperature, 51 g of acetic acid were then added, and the mixture was again heated to 70° C. At 70° C., 45 g of cyclopropylamine were then added dropwise. 100 ml of water were added to the reaction mixture which was stirred for 15 minutes, and the organic phase that formed was separated off. The organic phase was metered into a mixture of 89 g of potassium carbonate and 190 g of xylene (mixture of isomers) at from 140 to 142° C. The water of reaction that was liberated was separated off via a water separator. After all the water had been separated off, the mixture was cooled to 80° C. and, at a pressure of 40 mbar, xylene was distilled off. 80 g of 45% strength aqueous sodium hydroxide solution and 350 g of water were then added, and the remaining xylene was distilled off. After addition of 180 g of acetic acid and 100 g of water, the product was filtered off with suction and the solid was washed 3 times with 150 ml of water each time and 3 times with 200 ml of isopropanol each time. Drying under reduced pressure at 60° C. gave 170 g of 1-cyclopropyl-7-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinoline-carboxylic acid. This corresponds to a yield of 86% of theory.

WORKUP

后处理

  1. additionwas initially charged
  2. temperaturecooled to room temperature
  3. temperaturethe mixture was again heated to 70° C
  4. stirringwas stirred for 15 minutes
  5. customthe organic phase that formed
  6. customwas separated off
  7. additionThe organic phase was metered into a mixture of 89 g of potassium carbonate and 190 g of xylene (mixture of isomers) at from 140 to 142° C
  8. customThe water of reaction that
  9. customwas liberated was separated off via a water separator
  10. customAfter all the water had been separated off
  11. temperaturethe mixture was cooled to 80° C. and, at a pressure of 40 mbar, xylene
  12. distillationwas distilled off
  13. addition80 g of 45% strength aqueous sodium hydroxide solution and 350 g of water were then added
  14. distillationthe remaining xylene was distilled off
  15. additionAfter addition of 180 g of acetic acid and 100 g of water
  16. filtrationthe product was filtered off with suction
  17. washthe solid was washed 3 times with 150 ml of water each time and 3 times with 200 ml of isopropanol each time
  18. customDrying under reduced pressure at 60° C.