Water → HCID 67326247, 화합물

HRID 2199313노트

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HRID 2199313 반응식
[CH3:1][C:2]1[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:33])[C:15]2[CH:20]=[CH:19][C:18]([CH2:21][N:22]3[CH2:27][CH2:26][N:25]([CH3:28])[CH2:24][CH2:23]3)=[C:17]([C:29]([F:32])([F:31])[F:30])[CH:16]=2)=[CH:9][C:3]=1[C:4](OCC)=[O:5].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[O-]S([O-])(=O)=O.[Mg+2]>C1COCC1.C(OCC)C>[OH:5][CH2:4][C:3]1[CH:9]=[C:10]([NH:13][C:14](=[O:33])[C:15]2[CH:20]=[CH:19][C:18]([CH2:21][N:22]3[CH2:23][CH2:24][N:25]([CH3:28])[CH2:26][CH2:27]3)=[C:17]([C:29]([F:32])([F:30])[F:31])[CH:16]=2)[CH:11]=[CH:12][C:2]=1[CH3:1]

참가 물질

7

실험 절차

To a solution Ethyl 2-methyl-5-(4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)benzamido)benzoate (300 mg, 0.65 mmol) in dried THF (2.2 mL) was added Lithium aluminium hydride 2.0M THF solution (0.48 mL, 0.98 mmol) at 0° C. The reaction mixture was stirred for 2 hours at room temperature. When the reaction was completed, the reaction mixture was diluted with ethyl ether (2.0 mL) and added water very slowly to decompose the excess of the reagent. To a reaction mixture was added MgSO4, celite filtered and concentrated under reduced pressure. The title compound (230 mg, 84% yield) was used next step without further purification. MS m/z: 422 [M+1].

후처리

  1. filtrationfiltered
  2. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ac3fff0521a449d9b2b8851618c4571a
출처 데이터셋
uspto-grants-2016_06
특허 번호
US09358231B2

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