1,4-Dioxane → 9-[(2R,5S)-5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-3H-purin-6-one
反応式
O1CCOCC1.[PH2](O)=O.C(N1CCCCC1)C.CSC(O[C@@H:23]1[C@H:27](OC(SC)=S)[C@@H:26]([CH2:33][OH:34])[O:25][C@H:24]1[N:35]1[C:44]2[N:43]=[CH:42][N:41]=[C:39]([OH:40])[C:38]=2[N:37]=[CH:36]1)=S.CCCCCC.C(B(CC)CC)C>C(OCC)(=O)C.O1CCCC1>[C@@H:24]1([N:35]2[C:44]3[N:43]=[CH:42][N:41]=[C:39]([OH:40])[C:38]=3[N:37]=[CH:36]2)[O:25][C@H:26]([CH2:33][OH:34])[CH:27]=[CH:23]1参加物
実験手順
To a 1,4-dioxane solution containing N-ethylpiperidine hypophosphite (1.25 mL, 2.2 mmol) at a concentration of 1.764 mol/L, a mixed solution of a tetrahydrofuran solution (2 mL) of 2′,3′-bis-O-[(methylthio)thiocarbonyl]inosine (99 mg, 0.22 mmol) and a triethylborane hexane solution (0.22 mL, 0.22 mmol) at a concentration of 1.0 mol/L was added, and the obtained mixture was stirred at room temperature for one hour. The obtained reaction mixture was diluted with ethyl acetate. The resultant organic layer was washed with brine solution, and thereafter dried over anhydrous magnesium sulfate and concentrated under reduced pressure. After purification by chromatography (using as eluting solutions a mixed solvent of hexane and ethyl acetate (3:7), ethyl acetate, and a mixed solvent of dichloromethane and methanol (10:1) successively in this order), 47 mg of the intended product was obtained in a yield of 92%.
後処理
- customThe obtained reaction mixture
- washThe resultant organic layer was washed with brine solution
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customAfter purification by chromatography (
- washas eluting solutions a mixed solvent of hexane and ethyl acetate (3:7), ethyl acetate
出典と根拠
- ORDレコード
- ord-cdd400be304e40c9aafa970905d2eb90
- 出典データセット
- uspto-grants-2012_08
- 特許番号
- US08252920B2
反応ノート
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