Sodium Thiosulfate → HCID 178423543、化合物

HRID 1770644ノート

反応式

HRID 1770644 の反応式
[CH3:1][C:2]1[CH:14]=[C:13]([C:15]2[CH2:19][C@:18]([C:24]3[CH:29]=[C:28]([Cl:30])[C:27]([Cl:31])=[C:26]([Cl:32])[CH:25]=3)([C:20]([F:23])([F:22])[F:21])[O:17][N:16]=2)[CH:12]=[CH:11][C:3]=1[C:4]([NH:6][CH:7]1[CH2:10][S:9][CH2:8]1)=[O:5].C1C=C(Cl)C=C(C(OO)=[O:41])C=1.[O-]S([O-])(=S)=O.[Na+].[Na+]>ClCCl>[CH3:1][C:2]1[CH:14]=[C:13]([C:15]2[CH2:19][C@:18]([C:24]3[CH:29]=[C:28]([Cl:30])[C:27]([Cl:31])=[C:26]([Cl:32])[CH:25]=3)([C:20]([F:21])([F:22])[F:23])[O:17][N:16]=2)[CH:12]=[CH:11][C:3]=1[C:4]([NH:6][CH:7]1[CH2:8][S+:9]([O-:41])[CH2:10]1)=[O:5]

参加物

5

実験手順

To a suspension of 2-methyl-N-(thietan-3-yl)-4-[(5S)-5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]benzamide in dichloromethane (92 mL) was added m-CPBA (24.3 mmol, 5.58 g) portion wise at 0-5° C., and the reaction mixture was stirred for 10 min. A saturated Na2S2O3 solution was added, and the mixture was stirred for 10 min. The organic layer was washed with sat. NaHCO3 solution, water and brine, dried over MgSO4, filtered and evaporated. Purification over silica gel (eluent: CH2Cl2/EtOAc) yielded the title compound. LCMS (Method GR) 1.13 min, M+ 539/541; 1H NMR (400 MHz, CDCl3) 2.50 (s, 3H), 3.28 (m, 1H), 3.70 (d, 1H), 4.10-4.20 (m, 4H), 4.70 (m, 1H), 6.50 (d, 1H), 7.40-7.70 (1d+4s, 5H), 19F-NMR (CDCl3, 376 MHz): −79.43. Chiral HPLC Method Column: Daicel CHIRALPAK® IB, 3 μm, 0.46 cm×10 cm Mobile phase: Heptan/EtOH 80/20 Retention times of eluting isomers: 4.85 min (8.2%) 5.66 min (91.8%).

後処理

  1. stirringthe mixture was stirred for 10 min
  2. washThe organic layer was washed with sat. NaHCO3 solution, water and brine
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customevaporated
  6. customPurification over silica gel (eluent: CH2Cl2/EtOAc)

出典と根拠

ORDレコード
ord-0b0f37b3cfa840b0b6affb6e966be600
出典データセット
uspto-grants-2016_02
特許番号
US09247740B2

反応ノート

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