Methanol → HCID 10291255、化合物

HRID 1280727ノート

反応式

HRID 1280727 の反応式
[F:1][CH:2]([CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:3]([N:5]1[CH2:9][CH2:8][C@H:7]([S:10][C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)[CH2:6]1)=O.CO>C1COCC1>[F:1][CH:2]([CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:3][N:5]1[CH2:9][CH2:8][C@H:7]([S:10][C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=2)[CH2:6]1

参加物

4

反応条件

温度
0 °C

実験手順

(2RS,3S)-2-Fluoro-1-[3-(4-hydroxy-phenylsulfanyl)-pyrrolidin-1-yl]-4-phenyl-butan-1-one (200 mg, 0.56 mmol) was dissolved in THF (4 ml). Borane-dimethylsulfide complex (170 μl, 1.67 mmol) was added. The mixture was refluxed for 7 hours and then cooled to 0° C. MeOH (0.7 ml) was added dropwise and the solvent was removed in vacuo. The residue was dissolved with THF (3.5 ml) and 5N HCl (1.1 ml) and was stirred at 60° C. for 12 hours. The solvent was removed in vacuo and the residue was taken up in saturated NaHCO3 (3 ml). The aqueous layer was extracted with CH2Cl2 (3 times). The combined organic phases were dried over Na2SO4, filtered and the solvent was evaporated. The residue was chromatographed over silica gel (CH2Cl—MeOH, 99:1) to provide (2RS,3S)-4-[1-(2-fluoro-4-phenyl-butyl)-pyrrolidin-3-ylsulfanyl]-phenol (134 mg, 70%) as colorless oil. MS: m/e 346.3 (M+H+).

後処理

  1. additionBorane-dimethylsulfide complex (170 μl, 1.67 mmol) was added
  2. temperatureThe mixture was refluxed for 7 hours
  3. customthe solvent was removed in vacuo
  4. dissolutionThe residue was dissolved with THF (3.5 ml) and 5N HCl (1.1 ml)
  5. customThe solvent was removed in vacuo
  6. extractionThe aqueous layer was extracted with CH2Cl2 (3 times)
  7. dry with materialThe combined organic phases were dried over Na2SO4
  8. filtrationfiltered
  9. customthe solvent was evaporated
  10. customThe residue was chromatographed over silica gel (CH2Cl—MeOH, 99:1)

出典と根拠

ORDレコード
ord-9930e8a356014e8587ebd789c871e295
出典データセット
uspto-grants-2002_09
特許番号
US06451819B2

反応ノート

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