반응식
[O:1]=[C:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:16]=[CH:15][C:11]([C:12]([OH:14])=O)=[CH:10][CH:9]=2)[CH2:4][CH2:3]1.Cl.[CH3:18][O:19][C:20]([C:22]1([NH2:25])[CH2:24][CH2:23]1)=[O:21]>>[O:1]=[C:2]1[CH2:3][CH2:4][N:5]([C:8]2[CH:9]=[CH:10][C:11]([C:12]([NH:25][C:22]3([C:20]([O:19][CH3:18])=[O:21])[CH2:24][CH2:23]3)=[O:14])=[CH:15][CH:16]=2)[CH2:6][CH2:7]1참가 물질
3
실험 절차
The title compound was prepared from 4-(4-oxo-piperidine-1-yl)-benzoic acid (which was obtained in Example 151) and 1-aminocyclopropane-1-carboxylic acid methyl ester hydrochloride according to the procedure of Example 154 as a gum; MS (ES) m/z: 317.2 (MH+).
출처 및 근거
- ORD 기록
- ord-8523683106f24810960bfaff72308bbe
- 출처 데이터셋
- uspto-grants-2003_02
- 특허 번호
- US06525202B2
연결된 노트
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