Terephthalic Acid → N-(5-(4-Methoxyphenyl)-1H-pyrazol-3-yl)-N'-(5-(4-methylphenyl)-1H-pyrazol-3-yl)terephthalamide

HRID 2284240

Reaction equation

HRID 2284240 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.[NH2:15][C:16]1[CH:20]=[C:19]([C:21]2[CH:26]=[CH:25][C:24]([CH3:27])=[CH:23][CH:22]=2)[NH:18][N:17]=1.[C:28](O)(=[O:38])[C:29]1[CH:37]=[CH:36][C:32]([C:33](O)=[O:34])=[CH:31][CH:30]=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:28](=[O:38])[C:29]3[CH:37]=[CH:36][C:32]([C:33]([NH:15][C:16]4[CH:20]=[C:19]([C:21]5[CH:26]=[CH:25][C:24]([CH3:27])=[CH:23][CH:22]=5)[NH:18][N:17]=4)=[O:34])=[CH:31][CH:30]=3)[CH:6]=2)=[CH:8][CH:9]=1

Participants

4

Reactant 3

HCID 7489Terephthalic AcidHCID 7367685-Amino-3-(4-methylphenyl)pyrazoleHCID 27564693-Amino-5-(4-methoxyphenyl)pyrazole

Product 1

HCID 67112544N-(5-(4-Methoxyphenyl)-1H-pyrazol-3-yl)-N'-(5-(4-methylphenyl)-1H-pyrazol-3-yl)terephthalamide

Procedure

Compound 471 was prepared from 3-amino-5-(4-methoxyphenyl)pyrazole, 3-amino-5-(4-methylphenyl)pyrazole, and terephthalic acid. [M+H]+ calcd for C28H25N6O3: 493.20; found: 492.92.

Sources & evidence

ORD record
ord-95c8cb413dd643bdbded5a8b7cae9f06
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Linked notes

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