Ammonia → C-{3-(3-Fluoro-phenyl)-6-methoxy-1H-indazol-5-yl}-methylamine

HRID 1610154노트

반응식

HRID 1610154 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[Al+3].[Cl-].[Cl-].[F:11][C:12]1[CH:13]=[C:14]([C:18]2[C:26]3[C:21](=[CH:22][C:23]([O:29][CH3:30])=[C:24]([C:27]#[N:28])[CH:25]=3)[NH:20][N:19]=2)[CH:15]=[CH:16][CH:17]=1.N>O1CCCC1>[F:11][C:12]1[CH:13]=[C:14]([C:18]2[C:26]3[C:21](=[CH:22][C:23]([O:29][CH3:30])=[C:24]([CH2:27][NH2:28])[CH:25]=3)[NH:20][N:19]=2)[CH:15]=[CH:16][CH:17]=1

참가 물질

6

반응물 4

HCID 222AmmoniaHCID 6451240Aluminum(III) ChlorideHCID 21226445Aluminium lithium hydrideHCID 222607803-(3-Fluoro-phenyl)-6-methoxy-1H-indazole-5-carbonitrile

생성물 1

HCID 22260835C-{3-(3-Fluoro-phenyl)-6-methoxy-1H-indazol-5-yl}-methylamine수율 212.8%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A total of 71 mg of lithium aluminium hydride was suspended in 4.7 ml of tetrahydrofuran, 249 mg of aluminium chloride was added under ice-cooling, and the mixture was stirred for 10 minutes. To the reaction mixture was added 50 mg of 3-(3-fluoro-phenyl)-6-methoxy-1H-indazole-5-carbonitrile obtained in Production Example II-1-d, followed by stirring at room temperature for 3 hours. The reaction mixture was ice-cooled, 27% aqueous ammonia was added and the mixture was filtrated through Celite. The filtrate was evaporated, and the residue was purified and separated by silica gel column chromatography (NH silica gel) (ethyl acetate), to give 108 mg of the title compound.

후처리

  1. temperaturecooling
  2. stirringby stirring at room temperature for 3 hours
  3. temperaturecooled
  4. filtrationthe mixture was filtrated through Celite
  5. customThe filtrate was evaporated
  6. customthe residue was purified
  7. customseparated by silica gel column chromatography (NH silica gel) (ethyl acetate)

출처 및 근거

ORD 기록
ord-8709cacf20ad4ba19458f875fe9a1897
출처 데이터셋
uspto-grants-2006_01
특허 번호
US06982274B2

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