반응식
[C@@H:1]1([N:9]2[CH:16]=[CH:15][C:13]([NH2:14])=[N:12][C:10]2=[O:11])[O:8][C@H:5]([CH2:6][OH:7])[C@@H:3]([OH:4])[CH2:2]1.[CH3:17][C:18]([Si:21](Cl)([CH3:23])[CH3:22])([CH3:20])[CH3:19].CN(C=O)C>CO>[Si:21]([C@@:3]1([OH:4])[C@@H:5]([CH2:6][O:7][Si:21]([C:18]([CH3:20])([CH3:19])[CH3:17])([CH3:23])[CH3:22])[O:8][C@@H:1]([N:9]2[CH:16]=[CH:15][C:13]([NH2:14])=[N:12][C:10]2=[O:11])[CH2:2]1)([C:18]([CH3:20])([CH3:19])[CH3:17])([CH3:23])[CH3:22]참가 물질
5
실험 절차
2′-deoxycytidine dC (2.85 g, 12.54 mmol), imidiazole (6.49 g, 95.31 mmol), and TBSCl (7.18 g, 47.65 mmol) were added to anhydrous DMF (27 mL) and stirred at room temperature overnight under a N2 atmosphere. Methanol (20 mL) was added, and the mixture was stirred for 30 minutes and then concentrated in vacuo. Ethyl acetate (60 mL) and water (60 mL) were then added. The organic layer was separated and washed twice with water (20 mL), and the combined aqueous layer was extracted with ethyl acetate (20 mL). The combined organic layer was dried with Na2SO4, concentrated in vacuo, and purified by silica gel chromatography to give 3′,5′-O-bis-tert-butyldimethylsilyl-2′-deoxycytidine dC.01 (4.79 g, 84%) as a white foam.
후처리
- stirringthe mixture was stirred for 30 minutes
- concentrationconcentrated in vacuo
- additionEthyl acetate (60 mL) and water (60 mL) were then added
- customThe organic layer was separated
- washwashed twice with water (20 mL)
- extractionthe combined aqueous layer was extracted with ethyl acetate (20 mL)
- dry with materialThe combined organic layer was dried with Na2SO4
- concentrationconcentrated in vacuo
- custompurified by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-55f76d26021948b5b4db730e8061adb4
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07897737B2
연결된 노트
불러오는 중…