Terephthalic Acid → HCID 136352329, compound

HRID 2284166Notes

Reaction equation

HRID 2284166 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[NH:10][C:11]3[CH:17]=[C:16]([NH2:18])[CH:15]=[CH:14][C:12]=3[N:13]=2)=[CH:5][CH:4]=1.[C:19]([OH:30])(=O)[C:20]1[CH:28]=[CH:27][C:23]([C:24]([OH:26])=O)=[CH:22][CH:21]=1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[NH:13][C:12]3[CH:14]=[CH:15][C:16]([NH:18][C:24](=[O:26])[C:23]4[CH:22]=[CH:21][C:20]([C:19]([NH:18][C:16]5[CH:15]=[CH:14][C:12]6[NH:13][C:9]([C:6]7[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=7)=[N:10][C:11]=6[CH:17]=5)=[O:30])=[CH:28][CH:27]=4)=[CH:17][C:11]=3[N:10]=2)=[CH:7][CH:8]=1

Participants

3

Procedure

Compound 274 was prepared according to the procedure similar to that described in Scheme V from 2-(4-methoxyphenyl)-5-aminobenzimidazole and terephthalic acid. [M+H]+ calcd for C36H28N6O4: 609.22; found: 608.99.

Sources & evidence

ORD record
ord-7dab8c6a1a1c42c9bfa7db4bde2cc8a2
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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