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Cyanogen Bromide → (4S)-4-(3-Phenyl-butyl)-4,5-dihydro-oxazol-2-ylamine

HRID 1807901
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HRID 1807901 반응식
[NH2:1][C@@H:2]([CH2:5][CH2:6][CH:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:8])[CH2:3][OH:4].C([O-])(=O)C.[Na+].[N:20]#[C:21]Br>CO>[C:9]1([CH:7]([CH3:8])[CH2:6][CH2:5][C@H:2]2[CH2:3][O:4][C:21]([NH2:20])=[N:1]2)[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1
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참가 물질

5

반응물 3

HCID 10476Cyanogen BromideHCID 517045Sodium AcetateHCID 67177481(2S)-2-Amino-5-phenyl-hexan-1-ol

생성물 1

HCID 45101019(4S)-4-(3-Phenyl-butyl)-4,5-dihydro-oxazol-2-ylamine

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
0 °C

실험 절차

To a stirred solution of (2S)-2-amino-5-phenyl-hexan-1-ol (160 mg) in methanol (11 ml) at room temperature was added sodium acetate (136 mg). The mixture was cooled to 0° C. and a solution of cyanogen bromide (96 mg) in methanol (2 ml) was added dropwise. The mixture was stirred at 0° C. for 30 min and then at room temperature overnight before being concentrated in vacuo. The residue was resuspended in tetrahydrofuran/ethyl acetate (1/2) and washed sequentially with saturated aqueous sodium bicarbonate solution and saturated brine. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography (SiO2, heptane/dichloromethane/methanol gradient; eluant containing 1% aq. ammonia) to yield a colourlessoil, (128 mg, 71%); MS (ISP): 219.2 ([M+H]+).

후처리

  1. concentrationat room temperature overnight before being concentrated in vacuo
  2. washwashed sequentially with saturated aqueous sodium bicarbonate solution and saturated brine
  3. dry with materialThe organic layer was dried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography (SiO2, heptane/dichloromethane/methanol gradient; eluant containing 1% aq. ammonia)
  6. customto yield a colourlessoil, (128 mg, 71%)

출처 및 근거

ORD 기록
ord-f1f8f0f0b5134e7abe719959107419de
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08357712B2

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