반응식
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[NH2:34][C@@H:35]([C@H:46]([OH:55])[C:47]1[CH:52]=[CH:51][C:50]([O:53][CH3:54])=[CH:49][CH:48]=1)[C:36]([O:38][CH2:39][C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1)=[O:37].[NH:56]([C:63]([O:65][C:66]([CH3:69])([CH3:68])[CH3:67])=[O:64])[C@H:57]([C:60](O)=[O:61])[CH2:58][OH:59]>CN(C=O)C>[C:66]([O:65][C:63]([NH:56][C@@H:57]([CH2:60][OH:61])[C:58]([NH:34][C@@H:35]([C@H:46]([OH:55])[C:47]1[CH:52]=[CH:51][C:50]([O:53][CH3:54])=[CH:49][CH:48]=1)[C:36]([O:38][CH2:39][C:40]1[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=1)=[O:37])=[O:59])=[O:64])([CH3:69])([CH3:68])[CH3:67]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Sequentially HATU (645 mg, 1.70 mmol) and DIEA (0.99 mL, 5.7 mmol) were added to a 0° C. solution of (2S,3R)-benzyl 2-amino-3-hydroxy-3-(4-methoxyphenyl)propanoate (HCl salt, 477 mg, 1.41 mmol) and Boc-Ser-OH (290 mg, 1.41 mmol) in DMF (8 mL). The reaction mixture was allowed to warm to ambient temperature and stirred for 30 min. The mixture was concentrated and the residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=2:1) twice to afford (2S,3R)-benzyl 2-((S)-2-((tert-butoxycarbonyl)amino)-3-hydroxypropanamido)-3-hydroxy-3-(4-methoxyphenyl)propanoate (646 mg, 93% yield) as a colorless solid.
후처리
- concentrationThe mixture was concentrated
- customthe residue was purified by flash column chromatography on silica gel (petroleum ether/EtOAc=2:1) twice
출처 및 근거
- ORD 기록
- ord-514e7be395af4c72920394a73b5673db
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09434761B2
연결된 노트
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