Dimethylformamide dimethyl acetal → 5'-O-(t-Butyldimethylsilyl)-2',3'-dideoxy-3'-(N,N-dimethylaminomethylene)-2'-oxo-uridine
반응식
[Si:1]([O:8][CH2:9][C@H:10]1[O:14][C@@H:13]([N:15]2[CH:22]=[CH:21][C:19](=[O:20])[NH:18][C:16]2=[O:17])[C:12](=[O:23])[CH2:11]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].CO[CH:26](OC)[N:27]([CH3:29])[CH3:28]>CN(C)C=O>[Si:1]([O:8][CH2:9][C@H:10]1[O:14][C@@H:13]([N:15]2[CH:22]=[CH:21][C:19](=[O:20])[NH:18][C:16]2=[O:17])[C:12](=[O:23])[C:11]1=[CH:26][N:27]([CH3:29])[CH3:28])([C:4]([CH3:7])([CH3:5])[CH3:6])([CH3:2])[CH3:3]참가 물질
4
반응 조건
- 온도
- 50 °C
실험 절차
5'-O-(t-Butyldimethylsilyl)-2',3'-dideoxy-2'-oxo-uridine (2.2 g, 6.45 mmol) was dissolved in 25 mL of dry dimethylformamide (DMF) and 0.85 g (7.1 mmol) of N,N-dimethylformamide dimethyl acetal was added. The reaction mixture was heated to 50° C. under a nitrogen atmosphere and stirred for 0.5 h. The solvent was removed in vacuo and the residue (3.2 g) was dissolved in methylene chloride and purified by flash chromatography (5 psi) on a silica gel column (2×25 cm) eluted with 200 mL of methylene chloride, 200 mL of 2% methanol in methylene chloride and 200 mL of 5% methanol in methylene chloride to give 1.78 g (70% yield) of the title compound MS DCI: 396 (M+H)+, 418 (M+Na)+
후처리
- customThe solvent was removed in vacuo
- dissolutionthe residue (3.2 g) was dissolved in methylene chloride
- custompurified by flash chromatography (5 psi) on a silica gel column (2×25 cm)
- washeluted with 200 mL of methylene chloride, 200 mL of 2% methanol in methylene chloride and 200 mL of 5% methanol in methylene chloride
출처 및 근거
- ORD 기록
- ord-cbd6a5f1937042d793336d2de49f7ef8
- 출처 데이터셋
- uspto-grants-1997_01
- 특허 번호
- US05597824
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