Methylamine → (S)-tert-butyl 4-((R)-5-tert-butoxy-2-((methylamino)methyl)-5-oxopentyl)-2,2-dimethyloxazolidine-3-carboxylate
반응식
[C:1]([O:5][C:6](=[O:37])[CH2:7][CH2:8][C@@H:9]([CH2:25]OS(C1C=CC(C)=CC=1)(=O)=O)[CH2:10][C@H:11]1[CH2:15][O:14][C:13]([CH3:17])([CH3:16])[N:12]1[C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])([CH3:4])([CH3:3])[CH3:2].[CH3:38][NH2:39]>CCO>[C:1]([O:5][C:6](=[O:37])[CH2:7][CH2:8][C@@H:9]([CH2:25][NH:39][CH3:38])[CH2:10][C@H:11]1[CH2:15][O:14][C:13]([CH3:17])([CH3:16])[N:12]1[C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])([CH3:4])([CH3:3])[CH3:2]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 70 °C
실험 절차
(S)-tert-butyl 4-((R)-5-tert-butoxy-5-oxo-2-(tosyloxymethyl)pentyl)-2,2-dimethyloxazolidine-3-carboxylate (300 mg, 0.55 mmol) was dissolved in 30% MeNH2 in EtOH (60 mL), the solution was heated to 70° C. for 2 h in a pressure sealed vessel. After cooling to rt, the solvent was removed under reduced pressure to give (S)-tert-butyl 4-((R)-5-tert-butoxy-2-((methylamino)methyl)-5-oxopentyl)-2,2-dimethyloxazolidine-3-carboxylate (212 mg, 95%). MS ESI +ve m/z 401 (M+H).
후처리
- customsealed vessel
- temperatureAfter cooling to rt
- customthe solvent was removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-3c36ef59a7104325b6b6f899fd7d050b
- 출처 데이터셋
- uspto-grants-2013_07
- 특허 번호
- US08487108B2
반응 노트
불러오는 중…