반응식
Cl[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.[CH2:19]([O:21][NH2:22])[CH3:20]>>[CH2:19]([O:21][NH:22][C:12](=[O:14])[C:11]1[CH:15]=[CH:16][N:17]=[CH:18][C:10]=1[NH:9][C:3]1[CH:2]=[CH:7][C:6]([I:8])=[CH:5][CH:4]=1)[CH3:20]참가 물질
3
실험 절차
N-ethoxy-3-(4-iodo-phenylamino)-isonicotinamide was synthesized according to the procedure for General Method 1, outlined above, starting with 0.30 mmol of 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid (intermediate 2) and 0.40 mmol of O-ethyl-hydroxylamine LC/MS [9.14 min; 418 (M+1)]
출처 및 근거
- ORD 기록
- ord-301d0cf684664dc9b995ee6cf940a4a4
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08841459B2
연결된 노트
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