HCID 63748409, compound → HCID 67113662, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:21]=[CH:20][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:13][CH:12]=1)[N:6]=[CH:5]2.[OH:22][CH2:23][CH2:24][N:25]1[C:33]2[C:28](=[CH:29][C:30]([C:34](O)=[O:35])=[CH:31][CH:32]=2)[CH:27]=[CH:26]1>>[OH:22][CH2:23][CH2:24][N:25]1[C:33]2[C:28](=[CH:29][C:30]([C:34]([NH:1][C:2]3[CH:3]=[C:4]4[C:8](=[CH:9][CH:10]=3)[N:7]([C:11]3[CH:12]=[CH:13][C:14]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:20][CH:21]=3)[N:6]=[CH:5]4)=[O:35])=[CH:31][CH:32]=2)[CH:27]=[CH:26]1Participants
3
Procedure
Compound 1039 was prepared according to the procedure described in Scheme IV from ethyl 4-(5-amino-1H-indazol-1-yl)benzoate and 1-(2-hydroxyethyl)indole-5-carboxylic acid. [M+H]+ calcd for C27H24N4O4: 469.18; found 469.03.
Sources & evidence
- ORD record
- ord-a35b25fb6b1e4ca8b434b5dae72e9ee2
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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