Water → N-(3-{3-[3-(5-Fluoro-3-methyl-1H-indol-2-yl)propyl]-6-methyl-3-azabicyclo[3.1.0]hex-6-yl}phenyl)methanesulfonamide

HRID 428889노트

반응식

HRID 428889 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([CH2:11][CH2:12][C:13]([N:15]1[CH2:20][CH:19]3[CH:17]([C:18]3([C:22]3[CH:23]=[C:24]([NH:28][S:29]([CH3:32])(=[O:31])=[O:30])[CH:25]=[CH:26][CH:27]=3)[CH3:21])[CH2:16]1)=O)=[C:5]2[CH3:33].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.C(=O)([O-])O.[Na+]>O1CCCC1.C(OCC)(=O)C>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([CH2:11][CH2:12][CH2:13][N:15]1[CH2:20][CH:19]3[CH:17]([C:18]3([C:22]3[CH:23]=[C:24]([NH:28][S:29]([CH3:32])(=[O:31])=[O:30])[CH:25]=[CH:26][CH:27]=3)[CH3:21])[CH2:16]1)=[C:5]2[CH3:33]

참가 물질

7

실험 절차

To a solution of N-(3-{3-[3-(5-fluoro-3-methyl-1H-indol-2-yl)propanoyl]-6-methyl-3-azabicyclo[3.1.0]hex-6-yl}phenyl)methanesulfonamide (Preparation 128, 100 mg, 0.213 mmol) in anhydrous tetrahydrofuran (2.5 ml) under a nitrogen atmosphere at 0° C. was added dropwise lithium aluminium hydride (1.0M solution in tetrahydrofuran, 0.42 ml, 0.42 mmol) and the reaction mixture was stirred at room temperature overnight. The rapidly stirred reaction mixture was treated sequentially with water (0.45 ml), sodium hydrogen carbonate (450 mg) and ethyl acetate (10 ml). After 5 min, the reaction mixture was filtered and concentrated in vacuo to afford 95 mg of a colourless oil. This was purified by chromatography using a Biotage Flash 12™ cartridge packed with silica gel (8 g) eluting with hexane:ethyl acetate (100:0 to 0:100 over 30 min) then ethyl acetate methanol (100:0 to 0:100 over 15 min) to afford the title compound as a white foam (56 mg, 46%).

후처리

  1. customThe rapidly stirred reaction mixture
  2. waitAfter 5 min
  3. filtrationthe reaction mixture was filtered
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3ccd0cca904f441da7a80c00511f3ef9
출처 데이터셋
uspto-grants-2001_11
특허 번호
US06313312B1

반응 노트

불러오는 중…