Acetaldehyde → 3-{[3-(2-Chloro-pyrimidin-4-yl)-benzyl]-ethyl-amino}-azetidine-1-carboxylic acid tert-butyl ester
반응식
[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([NH:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]3[CH:25]=[CH:24][N:23]=[C:22]([Cl:26])[N:21]=3)[CH:15]=2)[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH:27](=O)[CH3:28]>>[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([N:12]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([C:20]3[CH:25]=[CH:24][N:23]=[C:22]([Cl:26])[N:21]=3)[CH:15]=2)[CH2:27][CH3:28])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]참가 물질
3
실험 절차
Intermediate 104 was coupled with acetaldehyde following procedure E. LC-MS showed the product had the expected M+H+ of 403.
출처 및 근거
- ORD 기록
- ord-cc46da1d786444f0b5b009eacc01e463
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07732444B2
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