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](O)=[O:13].C([O-])(=O)C.[NH4+:23]>>[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]([NH2:23])=[O:13]참가 물질
3
실험 절차
3-[(2-fluoro-4-iodophenyl)amino]isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 8 mmol of 3-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid (intermediate 1) and 16 mmol of ammonium acetate. LC/MS [7.27 min; 358 (M+1)].
후처리
- customLC/MS [7.27 min; 358 (M+1)]
출처 및 근거
- ORD 기록
- ord-2568ac6d5c60424286826a0cf3f7243e
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08524911B2
연결된 노트
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