Benzyl Bromide → (2S,3R,4R,5S,6R)-3,4,5-tris(benzyloxy)-2-methyl-6-(p-tolylthio)tetrahydro-2H-pyran

HRID 1745925ノート

反応式

HRID 1745925 の反応式
[C:1]([O:4][C@H:5]1[C@H:18]([O:19][C:20](=O)[CH3:21])[C@H:17]([O:23][C:24](=O)[CH3:25])[C@H:16]([CH3:27])[O:15][C@@H:6]1[S:7][C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=1)(=O)[CH3:2].C[O-].[Na+].CO.[H-].[Na+].[CH:35]1[CH:40]=[CH:39][C:38]([CH2:41]Br)=CC=1>CN(C=O)C.O.CCCCCC>[CH2:1]([O:4][C@H:5]1[C@H:18]([O:19][CH2:20][C:21]2[CH:5]=[CH:18][CH:17]=[CH:16][CH:27]=2)[C@H:17]([O:23][CH2:24][C:25]2[CH:41]=[CH:38][CH:39]=[CH:40][CH:35]=2)[C@H:16]([CH3:27])[O:15][C@@H:6]1[S:7][C:8]1[CH:9]=[CH:10][C:11]([CH3:14])=[CH:12][CH:13]=1)[C:2]1[CH:12]=[CH:13][CH:8]=[CH:9][CH:10]=1

参加物

8

実験手順

p-Methylphenyl 2,3,4-Tri-O-acetyl-1-thio-β-L-fucopyranoside (ibid, Brukart, M. D. et al. 1997) (2.5 g, 6.31 mmol) was treated with NaOMe-MeOH. The product was further treated with 85% NaH (463 g, 22.7 mmol) and BnBr (5.8 mL, 37.86 mmol) in DMF (25 mL). After reaction was finished, hexane (30 mL) and water (300 mL) were added into the vigorously stirred solution. The solid product was filtered, washed with water (2×5 mL) and hexane-AcOEt (15:1, 2×5 mL). The crude product was suspended in a hot (70° C.) mixture of AcOEt-Hexane (10:1), and stirred for 10 min, cooled to rt, filtered to gave pure 50 (2.6 g, 76%) as solid: [α]D22 +8° (c, 0.5, CHCl3); HRMS (M+Cs) calcd for C34H36O4SCs 672.1290. found 672.1287.

後処理

  1. customAfter reaction
  2. filtrationThe solid product was filtered
  3. washwashed with water (2×5 mL) and hexane-AcOEt (15:1, 2×5 mL)
  4. additionThe crude product was suspended in a hot (70° C.) mixture of AcOEt-Hexane (10:1)
  5. filtrationfiltered

出典と根拠

ORDレコード
ord-03486b7808ee4e40bf5e2ff89503d728
出典データセット
uspto-grants-2006_03
特許番号
US07019131B2

反応ノート

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