N-(5-amino-2-chlorophenyl)benzamide → N-(3-benzamido-4-chlorophenyl)-6-morpholinonicotinamide
반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([Cl:17])=[C:6]([NH:8][C:9](=[O:16])[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:7]=1.[O:18]1[CH2:23][CH2:22][N:21]([C:24]2[CH:32]=[CH:31][C:27]([C:28](O)=[O:29])=[CH:26][N:25]=2)[CH2:20][CH2:19]1>>[C:9]([NH:8][C:6]1[CH:7]=[C:2]([NH:1][C:28](=[O:29])[C:27]2[CH:31]=[CH:32][C:24]([N:21]3[CH2:20][CH2:19][O:18][CH2:23][CH2:22]3)=[N:25][CH:26]=2)[CH:3]=[CH:4][C:5]=1[Cl:17])(=[O:16])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1참가 물질
3
실험 절차
N-(5-amino-2-chlorophenyl)benzamide (0.24 mmol) was used in general procedure 2 with 6-morpholinonicotinic acid (0.30 mmol). The product was purified by RP-HPLC to give N-(3-benzamido-4-chlorophenyl)-6-morpholinonicotinamide. MS (Q1) 437.0 (M)+
후처리
- customThe product was purified by RP-HPLC
출처 및 근거
- ORD 기록
- ord-bf1f7403bd354735ae3fc8dab0f770ff
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08101610B2
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