2-Bromo-4'-methylacetophenone → 2-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridine

HRID 35516

반응식

HRID 35516 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][N:3]=1.Br[CH2:13][C:14]([C:16]1[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=1)=O>C(O)CC>[CH3:22][C:19]1[CH:20]=[CH:21][C:16]([C:14]2[N:1]=[C:2]3[CH:7]=[CH:6][C:5]([C:8]([F:9])([F:11])[F:10])=[CH:4][N:3]3[CH:13]=2)=[CH:17][CH:18]=1

참가 물질

4

반응물 2

HCID 692722-Bromo-4'-methylacetophenoneHCID 7358622-Amino-5-(trifluoromethyl)pyridine

생성물 1

HCID 139380372-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridine수율 70.2%

시약·촉매·용매 1

HCID 10311-Propanol용매

실험 절차

10 g (0.0616 mole) of 2-amino-5-trifluoromethylpyridine and 17.5 g (0.0616 mole) of 1-bromo-2-(4-methylphenyl)-2-ethanone are mixed in 200 ml of n-propanol and the solution is heated to reflux. At the end of the reaction, the reaction mixture is concentrated under reduced pressure and the evaporation residue taken up with water and treated with an excess of ammonia solution until the pH is basic. The imidazopyridine is extracted with dichloromethane and purified by chromatography. 11.95 g (56%) of white solid are obtained. M.p. 187°-188° C.

후처리

  1. temperaturethe solution is heated to reflux
  2. customAt the end of the reaction
  3. concentrationthe reaction mixture is concentrated under reduced pressure
  4. additiontreated with an excess of ammonia solution until the pH
  5. extractionThe imidazopyridine is extracted with dichloromethane
  6. custompurified by chromatography

출처 및 근거

ORD 기록
ord-20bd24ff2e884f868dd93e00939014f6
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04767755

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