반응식
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C@H:12]([NH:23][C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])[C:13]([NH:15][C@@H:16]([CH:20]([CH3:22])[CH3:21])C(O)=O)=[O:14])=[CH:7][CH:6]=1)[CH:2]=[CH2:3].C[N:32]([C:34]([O:38]N1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)[CH:58]([CH3:60])[CH3:59].C[CH2:65][O:66][C:67]([CH3:69])=[O:68]>CN(C=O)C>[CH3:65][O:66][C:67](=[O:68])[C@@H:69]([NH:32][C:34](=[O:38])[C@@H:16]([NH:15][C:13](=[O:14])[C@@H:12]([NH:23][C:24]([O:26][C:27]([CH3:28])([CH3:30])[CH3:29])=[O:25])[CH2:11][C:8]1[CH:7]=[CH:6][C:5]([O:4][CH2:1][CH:2]=[CH2:3])=[CH:10][CH:9]=1)[CH:20]([CH3:22])[CH3:21])[CH2:60][CH:58]=[CH2:59]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
Carboxylic acid 43 (1.00 g, 2.38 mmol), HATU (2.62 mmol) and (S)-allyl-glycine methyl ester hydrochloride (2.62 mmol) were dissolved in DMF (30 mL). DIPEA was added (9.52 mmol) and the reaction mixture was stirred at rt for 18 h before being partitioned between EtOAc and 1M hydrochloric acid. The organic phase was washed sequentially with 1M hydrochloric acid and brine before being dried (MgSO4), filtered and concentrated in vacuo. Purification was achieved using flash chromatography, eluting with a gradient of EtOAc and (50/70) petroleum ether to yield a white solid, 1.05 g, 83%. Rf=0.48 (1/1 EtOAc/(50/70) petroleum ether). m.p. 106-108° C.
후처리
- custombefore being partitioned between EtOAc and 1M hydrochloric acid
- washThe organic phase was washed sequentially with 1M hydrochloric acid and brine
- dry with materialbefore being dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customPurification
- washeluting with a gradient of EtOAc and (50/70) petroleum ether
- customto yield a white solid, 1.05 g, 83%
출처 및 근거
- ORD 기록
- ord-57570430308e4a12bc8ce5b51ca9d9a9
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09434762B2
연결된 노트
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