반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])[CH:5]=[CH:6][CH:7]=1.[C:14]1([CH2:20][O:21][C:22]([NH:24][C@H:25]([C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])[CH2:26][CH2:27]O)=[O:23])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C[N+](CC(O)=O)(C)C>>[CH3:35][C:32]([CH3:33])([O:31][C:29](=[O:30])[CH:25]([NH:24][C:22]([O:21][CH2:20][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:23])[CH2:26][CH2:27][O:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][C:10]([O:12][CH3:13])=[O:11])[CH:5]=[CH:6][CH:7]=1)[CH3:34]참가 물질
4
실험 절차
The operation is carried out as in Preparation 1 (Method 2) starting from 270 mg of the phenol prepared in Stage A, 309 mg of 1,1-dimethyl-ethyl N-[(phenylmethoxy)carbonyl]-L-homoserinate and 616 mg of betaine. 320 mg of expected product is obtained.
후처리
- customThe operation is carried out as in Preparation 1 (Method 2)
출처 및 근거
- ORD 기록
- ord-cedc6fdd6cc44c19875c49c35baec381
- 출처 데이터셋
- uspto-grants-2003_08
- 특허 번호
- US06602878B1
연결된 노트
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