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Cesium carbonate → (S)-3-((S)-3-(4-(4-Bromo-3-(trifluoromethoxy)benzyloxy)-phenyl)-3-(isoxazol-3-yl)propanoyl)-4-benzyloxazolidin-2-one

HRID 2235605
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HRID 2235605 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][OH:9])=[CH:4][C:3]=1[O:10][C:11]([F:14])([F:13])[F:12].S(Br)(Br)=O.[CH2:19]([C@H:26]1[CH2:30][O:29][C:28](=[O:31])[N:27]1[C:32](=[O:47])[CH2:33][C@@H:34]([C:40]1[CH:45]=[CH:44][C:43](O)=[CH:42][CH:41]=1)[C:35]1[CH:39]=[CH:38][O:37][N:36]=1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C([O-])([O-])=O.[Cs+].[Cs+]>C(Cl)Cl.CN(C=O)C.CCOC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][O:9][C:43]2[CH:42]=[CH:41][C:40]([C@@H:34]([C:35]3[CH:39]=[CH:38][O:37][N:36]=3)[CH2:33][C:32]([N:27]3[C@@H:26]([CH2:19][C:20]4[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=4)[CH2:30][O:29][C:28]3=[O:31])=[O:47])=[CH:45][CH:44]=2)=[CH:4][C:3]=1[O:10][C:11]([F:13])([F:12])[F:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

HCID 10796Cesium carbonateHCID 68176Thionyl bromideHCID 54472733(4-Bromo-3-(trifluoromethoxy)phenyl)methanolHCID 57801829(S)-4-Benzyl-3-((S)-3-(4-hydroxyphenyl)-3-(isoxazol-3-yl)propanoyl)oxazolidin-2-one

생성물 1

HCID 59300650(S)-3-((S)-3-(4-(4-Bromo-3-(trifluoromethoxy)benzyloxy)-phenyl)-3-(isoxazol-3-yl)propanoyl)-4-benzyloxazolidin-2-one

시약·촉매·용매 3

HCID 6228Dimethylformamide용매2회HCID 6344Dichloromethane용매HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 28.3 (1.30 g, 4.80 mmol), thionyl bromide (1.01 g, 4.84 mmol), and DMF (0.1 mL) in DCM (8.0 mL) was stirred at room temperature for 50 minutes. The solvent was then removed. To the residue was added 7.5 (1.10 g, 2.80 mmol) and Cs2CO3 (1.10 g, 3.36 mmol) in DMF (8.0 mL). The mixture was stirred at room temperature for 4 hours. EtOAc (150 mL) was added, and the mixture was washed with brine (25×3 mL) and dried with MgSO4. The solvent was removed, and the crude product was purified by CombiFlash, eluting with EtOAc and hexane, to give the title compound 28.4. 1H NMR (CDCl3) δ 2.77 (dd, J=4.2, 9.5 Hz, 1H), 3.21 (dd, J=4.2, 9.5 Hz, 1H), 3.52 (dd, J=8.6, 17.6 Hz, 1H), 4.04 (dd, J=8.6, 17.6 Hz, 1H), 4.63 (m, 1H), 4.76 (m, 1H), 5.01 (s, 2H), 6.14 (d, J=1.5 Hz, 1H), 6.92 (d, J=6.9, Hz, 2H), 7.20-7.35 (m, 9H), 7.64 (d, J=8.3, Hz, 1H), 8.31 (d, J=1.5 Hz, 1H). MS ESI (pos.) m/e: 647 (M+H).

후처리

  1. customThe solvent was then removed
  2. stirringThe mixture was stirred at room temperature for 4 hours
  3. washthe mixture was washed with brine (25×3 mL)
  4. dry with materialdried with MgSO4
  5. customThe solvent was removed
  6. customthe crude product was purified by CombiFlash
  7. washeluting with EtOAc and hexane

출처 및 근거

ORD 기록
ord-f089181fa7a94b4a84a653d1a88ba779
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07714008B2

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