1-benzyl-1H-indazol-4-amine → N-(1-benzyl-1H-indazol-4-yl)-7-methoxyimidazo[1,2-a]pyridine-3-carboxamide
Reaction equation
F[C:2]1[CH:18]=[C:17](F)[CH:16]=[CH:15][C:3]=1[CH2:4][N:5]1[C:13]2[CH:12]=[CH:11][CH:10]=[C:9]([NH2:14])[C:8]=2[CH:7]=[N:6]1.[CH3:20][O:21][C:22]1[CH:27]=[CH:26][N:25]2[C:28]([C:31](O)=[O:32])=[CH:29][N:30]=[C:24]2[CH:23]=1.C(N1C2C=CC=C(N)C=2C=N1)C1C=CC=CC=1>>[CH2:4]([N:5]1[C:13]2[C:8](=[C:9]([NH:14][C:31]([C:28]3[N:25]4[CH:26]=[CH:27][C:22]([O:21][CH3:20])=[CH:23][C:24]4=[N:30][CH:29]=3)=[O:32])[CH:10]=[CH:11][CH:12]=2)[CH:7]=[N:6]1)[C:3]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:2]=1Participants
4
Procedure
Prepared according to the method of Example 109, replacing 7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxylic acid and 1-(2,4-difluorobenzyl)-1H-indazol-4-amine with 7-methoxyimidazo[1,2-a]pyridine-3-carboxylic acid and 1-benzyl-1H-indazol-4-amine, respectively. MS (APCI) m/z=398 (M+H).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-bfdd75ea6af5499db2bcaf4cdd6b4859
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09174981B2
Reaction notes
Loading…