Hydrochloric Acid → (5R)-3-(4-{1-[(2S)-2,3-Dihydroxypropanoyl]-1,2,3,6-tetrahydropyridin-4-yl}-3,5-difluorophenyl)-5-[(4-methyl-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one

HRID 1452604노트

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HRID 1452604 반응식
CC1(C)[O:6][C@H:5]([C:7]([N:9]2[CH2:14][CH:13]=[C:12]([C:15]3[C:20]([F:21])=[CH:19][C:18]([N:22]4[CH2:26][C@H:25]([CH2:27][N:28]5[CH:32]=[C:31]([CH3:33])[N:30]=[N:29]5)[O:24][C:23]4=[O:34])=[CH:17][C:16]=3[F:35])[CH2:11][CH2:10]2)=[O:8])[CH2:4][O:3]1.Cl.C(OCC)(=O)C>O1CCCC1>[OH:6][C@@H:5]([CH2:4][OH:3])[C:7]([N:9]1[CH2:10][CH:11]=[C:12]([C:15]2[C:20]([F:21])=[CH:19][C:18]([N:22]3[CH2:26][C@H:25]([CH2:27][N:28]4[CH:32]=[C:31]([CH3:33])[N:30]=[N:29]4)[O:24][C:23]3=[O:34])=[CH:17][C:16]=2[F:35])[CH2:13][CH2:14]1)=[O:8]

참가 물질

5

실험 절차

(5R)-3-[4-(1-{[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]carbonyl}-1,2,3,6-tetrahydropyridin-4-yl)-3,5-difluorophenyl]-5-[(4-methyl-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one (Intermediate 55) (542 mg, 1.08 mmol) was dissolved in tetrahydrofuran (20 ml). A solution of hydrochloric acid (1N, 10 ml) was added and the reaction mixture was stirred at room temperature. After 64 hours, the solution was poured into ethyl acetate the aqueous was extracted with ethyl acetate. The aqueous was basified with a solution of 10% aqueous sodium acetate and re-extracted with ethyl acetate. The combined organics were dried over magnesium sulfate and concentrated under vacuum. Chromatography on silica gel with 10% methanol in ethyl acetate gave 254 mg of the title product.

후처리

  1. extractionaqueous was extracted with ethyl acetate
  2. extractionre-extracted with ethyl acetate
  3. dry with materialThe combined organics were dried over magnesium sulfate
  4. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-f62889baa39d47538d91e8c6fd9c1ce9
출처 데이터셋
uspto-grants-2009_01
특허 번호
US07473699B2

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