4-(2-Hydroxyethoxy)benzenecarboxylic acid → HCID 67113342, 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:16]=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=1)[N:6]=[CH:5]2.[OH:18][CH2:19][CH2:20][O:21][C:22]1[CH:30]=[CH:29][C:25]([C:26](O)=[O:27])=[CH:24][CH:23]=1>>[OH:18][CH2:19][CH2:20][O:21][C:22]1[CH:30]=[CH:29][C:25]([C:26]([NH:17][C:14]2[CH:15]=[CH:16][C:11]([N:7]3[C:8]4[C:4](=[CH:3][C:2]([NH:1][C:26](=[O:27])[C:25]5[CH:29]=[CH:30][C:22]([O:21][CH2:20][CH2:19][OH:18])=[CH:23][CH:24]=5)=[CH:10][CH:9]=4)[CH:5]=[N:6]3)=[CH:12][CH:13]=2)=[O:27])=[CH:24][CH:23]=1Participants
3
Procedure
Compound 995 was prepared according to the procedure described in Scheme IV from 5-amino-1-(4-aminophenyl)indazole and 4-(2-hydroxyethoxy)benzoic acid. [M+H]+ calcd for C31H29N4O6: 553.21; found: 553.10.
Sources & evidence
- ORD record
- ord-033962c52e4f4a26a1a94fb0da658ce9
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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