Terephthalic Acid → HCID 67114005, compound
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]([OH:26])(=O)[C:16]1[CH:24]=[CH:23][C:19]([C:20]([OH:22])=O)=[CH:18][CH:17]=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:20](=[O:22])[C:19]3[CH:18]=[CH:17][C:16]([C:15]([NH:1][C:2]4[CH:6]=[C:5]([C:7]5[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=5)[NH:4][N:3]=4)=[O:26])=[CH:24][CH:23]=3)[CH:6]=2)=[CH:8][CH:9]=1Participants
3
Procedure
Compound 473 was prepared from 3-amino-5-(4-methoxyphenyl)pyrazole and terephthalic acid. [M+H]+ calcd for C28H25N6O4: 509.19; found: 508.91.
Sources & evidence
- ORD record
- ord-9da0de9b2788443a91e1e67b4a0b3576
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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