Hydrochloric Acid → 2-Chloro-6-(trifluoromethoxy)-1,3-benzothiazole

HRID 9568

반응식

HRID 9568 반응식
N(OCCC(C)C)=O.[F:9][C:10]([F:23])([F:22])[O:11][C:12]1[CH:21]=[CH:20][C:15]2[N:16]=[C:17](N)[S:18][C:14]=2[CH:13]=1.[ClH:24]>C(#N)C.[Cu](Cl)Cl>[Cl:24][C:17]1[S:18][C:14]2[CH:13]=[C:12]([O:11][C:10]([F:23])([F:22])[F:9])[CH:21]=[CH:20][C:15]=2[N:16]=1

참가 물질

6

실험 절차

To a solution containing dry copper (II) chloride (3.44 g, 25.62 mmol) and tri(ethylene glycol) dimethyl ether (10 g) in acetonitrile (150 mL) was added isoamyl nitrite (4.5 mL, 32.02 mmol). The reaction mixture was stirred at rt under argon for 30 minutes. To this suspension was added dropwise, a solution containing 6-trifluoromethoxy-1,3-benzothiazol-2-ylamine (5 g, 21.35 mmol) and tri(ethylene glycol) dimethyl ether (10 g). The reaction mixture was stirred at rt for 10 minutes, and then heated at 50° C. for 3 h. The mixture was cooled to rt, poured cautiously into aqueous 6 N HCl, and extracted with ethyl acetate. The organic layer was washed with 1N aqueous HCl and brine, and concentrated under reduced pressure to give the desired compound in near-quantitative yield, which was used without further purification in the next step.

후처리

  1. additionTo this suspension was added dropwise
  2. stirringThe reaction mixture was stirred at rt for 10 minutes
  3. temperatureheated at 50° C. for 3 h
  4. temperatureThe mixture was cooled to rt
  5. extractionextracted with ethyl acetate
  6. washThe organic layer was washed with 1N aqueous HCl and brine
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-405e37b0937d460898462bc7780bccea
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091228B2

연결된 노트

불러오는 중…