반응식
[CH2:1]([O:8][CH2:9][C@@H:10]([NH:14][C:15](OC(C)(C)C)=O)[C:11]([OH:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.IC.[H-].[Na+].C(O)(=O)[CH2:27][C:28]([CH2:33]C(O)=O)([C:30](O)=O)[OH:29].[O:39]1CCC[CH2:40]1>>[CH2:1]([O:8][CH2:9][C@@H:10]([NH:14][CH2:15][C:40]([O:29][C:28]([CH3:27])([CH3:30])[CH3:33])=[O:39])[C:11]([OH:13])=[O:12])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
(2R)-3-Benzyloxy-2-tert-butoxycarbonylaminopropionic acid (7.0 g; 23.7 mmol) was dissolved in dry tetrahydrofuran and iodomethane (11.9 mL; 189 mmol) was added. The reaction mixture was cooled to OIC and sodium hydride (60% in mineral oil) (2.73 g; 71 mmol) was added. The reaction mixture was left 3 days without stirring at 0° C. Citric acid (5%) was added until pH 2.5. Tetrahydrofuran was removed in vacuo and the residue was extracted with methylene chloride (3×100 mL). The organic phase was dried (magnesium sulfate) and evaporated in vacuo. The residue was dissolved in diethyl ether (20 mL) and dicyclohexylamine (10 mL) and is heptane (100 mL) were added. The reaction mixture was left 3 days without stirring at 0° C. The reaction mixture was filtered to afford 5.78 g of (2R)-3-benzyloxy-2-(tert-butoxycarbonylmethylamino)propionic acid.
후처리
- additionwas added
- customTetrahydrofuran was removed in vacuo
- extractionthe residue was extracted with methylene chloride (3×100 mL)
- dry with materialThe organic phase was dried (magnesium sulfate)
- customevaporated in vacuo
- dissolutionThe residue was dissolved in diethyl ether (20 mL)
- additionwere added
- waitThe reaction mixture was left 3 days
- stirringwithout stirring at 0° C
- filtrationThe reaction mixture was filtered
출처 및 근거
- ORD 기록
- ord-f5b5b9ca84d0473083802f5be213249f
- 출처 데이터셋
- uspto-grants-2005_09
- 특허 번호
- US06939880B2
연결된 노트
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