반응식
[F:1][C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10]1[CH:18]=[N:17][CH:16]=[CH:15][C:11]=1[C:12]([OH:14])=O.[Cl:19][CH2:20][CH2:21][CH2:22][NH2:23]>>[Cl:19][CH2:20][CH2:21][CH2:22][NH:23][C:12](=[O:14])[C:11]1[CH:15]=[CH:16][N:17]=[CH:18][C:10]=1[NH:9][C:3]1[CH:4]=[CH:5][C:6]([I:8])=[CH:7][C:2]=1[F:1]참가 물질
3
실험 절차
N-(3-chloropropyl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 1 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 1.3 mmol of 3-chloropropylamine. LC/MS [9.24 min; 434 (M+1)]
후처리
- customLC/MS [9.24 min; 434 (M+1)]
출처 및 근거
- ORD 기록
- ord-4a6d5745b26947f79e5869e663758dab
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08524911B2
연결된 노트
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