Hydrochloric Acid → N4-{4-[(3-Cyclopropyl-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluorophenyl}-6-(trifluoromethyl)pyrimidine-2,4-diamine

HRID 2192185노트

반응식

HRID 2192185 반응식
[CH:1]1([C:4]2[C:12]3[C:7](=[N:8][CH:9]=[CH:10][C:11]=3[O:13][C:14]3[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][C:15]=3[F:21])[NH:6][CH:5]=2)[CH2:3][CH2:2]1.Cl[C:23]1[CH:28]=[C:27]([C:29]([F:32])([F:31])[F:30])[N:26]=[C:25]([NH2:33])[N:24]=1.Cl.[OH-].[Na+]>O>[CH:1]1([C:4]2[C:12]3[C:7](=[N:8][CH:9]=[CH:10][C:11]=3[O:13][C:14]3[CH:20]=[CH:19][C:17]([NH:18][C:23]4[CH:28]=[C:27]([C:29]([F:32])([F:30])[F:31])[N:26]=[C:25]([NH2:33])[N:24]=4)=[CH:16][C:15]=3[F:21])[NH:6][CH:5]=2)[CH2:3][CH2:2]1

참가 물질

6

실험 절차

114 mg (0.40 mmol) of 4-[(3-cyclopropyl-1H-pyrrolo[2,3-b]pyridin-4-yl)oxy]-3-fluoroaniline and 95 mg (0.48 mmol) of 4-chloro-6-(trifluoromethyl)pyrimidine-2-amine are suspended in 3.5 ml of water. 0.52 ml (0.52 mmol) of 1N hydrochloric acid are added, and the mixture is heated at reflux overnight. Another 30 mg (0.15 mmol) of 4-chloro-6-(trifluoromethyl)pyrimidine-2-amine are then added, and the mixture is heated for another 6 hours. By addition of 1N aqueous sodium hydroxide solution, the pH is adjusted to 10, resulting in the precipitation of crystals. The crystals are filtered off with suction and purified by chromatography on silica gel (mobile phase: dichloromethane/methanol (7N ammonia) 100:1 to 100:3).

후처리

  1. temperaturethe mixture is heated
  2. temperatureat reflux overnight
  3. temperaturethe mixture is heated for another 6 hours
  4. customresulting in the precipitation of crystals
  5. filtrationThe crystals are filtered off with suction
  6. custompurified by chromatography on silica gel (mobile phase: dichloromethane/methanol (7N ammonia) 100:1 to 100:3)

출처 및 근거

ORD 기록
ord-12377dd186ee482bb37391b3a8b567ff
출처 데이터셋
uspto-grants-2012_12
특허 번호
US08329716B2

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