Hydroxylamine → (R)-6-(4-Fluoro-3-methylbenzyloxy)-2-(4-fluoro-3-methylphenoxy)-N-hydroxyhexanamide

HRID 1361062노트

반응식

HRID 1361062 반응식
[F:1][C:2]1[CH:34]=[CH:33][C:5]([CH2:6][O:7][CH2:8][CH2:9][CH2:10][CH2:11][C@@H:12]([O:24][C:25]2[CH:30]=[CH:29][C:28]([F:31])=[C:27]([CH3:32])[CH:26]=2)[C:13]([N:15]2[C@@H](C(C)C)COC2=O)=[O:14])=[CH:4][C:3]=1[CH3:35].C[OH:37].NO.[C-]#N.[K+]>C1COCC1.O>[F:1][C:2]1[CH:34]=[CH:33][C:5]([CH2:6][O:7][CH2:8][CH2:9][CH2:10][CH2:11][C@@H:12]([O:24][C:25]2[CH:30]=[CH:29][C:28]([F:31])=[C:27]([CH3:32])[CH:26]=2)[C:13]([NH:15][OH:37])=[O:14])=[CH:4][C:3]=1[CH3:35]

참가 물질

7

실험 절차

To a solution of (S)-3-((R)-6-(4-fluoro-3-methylbenzyloxy)-2-(4-fluoro-3-methylphenoxy)hexanoyl)-4-isopropyloxazolidin-2-one (100 mg, 0.20 mmol) dissolved in 2 mL of THF, methanol, and 50 wt % NH2OH in H2O (2:2:1) was added KCN (4.0 mg, 0.06 mmol). The resulting mixture stirred for 3 days at room temperature. The reaction was quenched by the addition of 1M aqueous HCl (10 mL) and the resulting mixture extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine (2×5 mL). The product was isolated by flash column chromatography eluting with 0% to 10% methanol/DCM to give the title compound (54.2 mg) as colorless oil.

후처리

  1. customThe reaction was quenched by the addition of 1M aqueous HCl (10 mL)
  2. extractionthe resulting mixture extracted with ethyl acetate (3×10 mL)
  3. washThe combined organic layers were washed with brine (2×5 mL)
  4. customThe product was isolated by flash column chromatography
  5. washeluting with 0% to 10% methanol/DCM

출처 및 근거

ORD 기록
ord-3a31da602e3945f29029b08a105a5d14
출처 데이터셋
uspto-grants-2011_02
특허 번호
US07879911B2

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