Chloroacetyl chloride → 2-chloro-N-(5-chloropyridin-2-yl)acetamide

HRID 491819

반응식

HRID 491819 반응식
[Cl:1][CH2:2][C:3](Cl)=[O:4].[NH2:6][C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][N:8]=1.C(N(CC)CC)C>ClCCl>[Cl:1][CH2:2][C:3]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][N:8]=1)=[O:4]

참가 물질

5

실험 절차

Chloroacetyl chloride (95.5 ml) is dissolved in dichloromethane (500 ml), and thereto is added dropwise a suspension of 2-amino-5-chloropyridine (128.6 g) and triethylamine (169 ml) in dichloromethane (1000 ml) under ice-cooling, and the reaction solution is warmed to room temperature, and stirred for 0.5 hours. The reaction solution is concentrated under reduced pressure, thereto is poured ice-water, and then the reaction mixture is extracted with ethyl acetate. The organic layer is washed with saturated brine, dried over sodium sulfate and treated with activated charcoal. After filtration to remove insoluble materials, the filtrate is concentrated under reduced pressure and the resulting residue is suspended in diisopropyl ether. The precipitates are collected by filtration, washed with diisopropyl ether and dried to give 2-chloro-N-(5-chloropyridin-2-yl)acetamide (153.4 g).

후처리

  1. additionis added dropwise
  2. temperaturecooling
  3. concentrationThe reaction solution is concentrated under reduced pressure
  4. additionis poured ice-water
  5. extractionthe reaction mixture is extracted with ethyl acetate
  6. washThe organic layer is washed with saturated brine
  7. dry with materialdried over sodium sulfate
  8. additiontreated with activated charcoal
  9. filtrationAfter filtration
  10. customto remove insoluble materials
  11. concentrationthe filtrate is concentrated under reduced pressure
  12. filtrationThe precipitates are collected by filtration
  13. washwashed with diisopropyl ether
  14. customdried

출처 및 근거

ORD 기록
ord-b62eb539d4684876bd3c42f6b68673aa
출처 데이터셋
uspto-grants-2009_05
특허 번호
US07531537B2

연결된 노트

불러오는 중…