Reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=2)[NH:4][N:3]=1.[C:15]1([C:24]2[CH:29]=[CH:28][C:27]([C:30]([OH:32])=O)=[CH:26][CH:25]=2)[CH:20]=[CH:19][C:18]([C:21]([OH:23])=O)=[CH:17][CH:16]=1>>[CH3:14][O:13][C:10]1[CH:11]=[CH:12][C:7]([C:5]2[NH:4][N:3]=[C:2]([NH:1][C:30]([C:27]3[CH:26]=[CH:25][C:24]([C:15]4[CH:16]=[CH:17][C:18]([C:21]([NH:1][C:2]5[CH:6]=[C:5]([C:7]6[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=6)[NH:4][N:3]=5)=[O:23])=[CH:19][CH:20]=4)=[CH:29][CH:28]=3)=[O:32])[CH:6]=2)=[CH:8][CH:9]=1Participants
3
Procedure
Compound 474 was prepared from 3-amino-5-(4-methoxyphenyl)pyrazole and biphenyl-4,4′-dicarboxylic acid. [M+H]+ calcd for C34H29N6O4: 585.23; found: 585.01.
Sources & evidence
- ORD record
- ord-2a2ab0bc719b4279bc30ea13c7b62ae1
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Linked notes
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