Methylamine → 2-{4-[(1-Cyclopentylpiperidin-4-yl)oxy]phenyl}-8-fluoro-3-methylquinazolin-4(3H)-one
반응식
[NH2:1][C:2]1[C:10]([F:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH3:12][NH2:13].[CH:14]1([N:19]2[CH2:24][CH2:23][CH:22]([O:25][C:26]3[CH:33]=[CH:32][C:29]([CH:30]=O)=[C:28](OC)[CH:27]=3)[CH2:21][CH2:20]2)[CH2:18][CH2:17][CH2:16][CH2:15]1>>[CH:14]1([N:19]2[CH2:24][CH2:23][CH:22]([O:25][C:26]3[CH:33]=[CH:32][C:29]([C:30]4[N:13]([CH3:12])[C:4](=[O:6])[C:3]5[C:2](=[C:10]([F:11])[CH:9]=[CH:8][CH:7]=5)[N:1]=4)=[CH:28][CH:27]=3)[CH2:21][CH2:20]2)[CH2:18][CH2:17][CH2:16][CH2:15]1참가 물질
4
실험 절차
The entitled compound was obtained according to the method of Example 15 but starting from 2-amino-3-fluorobenzoic acid, methylamine and 4-[(1-cyclopentylpiperidin-4-yl)oxy]-2-methoxybenzaldehyde.
후처리
- customThe entitled compound was obtained
출처 및 근거
- ORD 기록
- ord-e58551f795a14b1d950bd10c26da6a12
- 출처 데이터셋
- uspto-grants-2011_06
- 특허 번호
- US07960394B2
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