4-Aminobenzoic acid hydrazide → HCID 178482659, compound

HRID 2284167Notes

Reaction equation

HRID 2284167 reaction equation
[CH3:1][N:2]([CH3:21])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[NH:10][C:11]3[CH:17]=[C:16]([C:18]([OH:20])=O)[CH:15]=[CH:14][C:12]=3[N:13]=2)=[CH:5][CH:4]=1.[NH2:22][C:23]1[CH:32]=[CH:31][C:26]([C:27]([NH:29][NH2:30])=[O:28])=[CH:25][CH:24]=1>>[CH3:21][N:2]([CH3:1])[C:3]1[CH:4]=[CH:5][C:6]([C:9]2[NH:13][C:12]3[CH:14]=[CH:15][C:16]([C:18]([NH:22][C:23]4[CH:24]=[CH:25][C:26]([C:27]([NH:29][NH2:30])=[O:28])=[CH:31][CH:32]=4)=[O:20])=[CH:17][C:11]=3[N:10]=2)=[CH:7][CH:8]=1

Participants

3

Reactant 2

HCID 214504-Aminobenzoic acid hydrazideHCID 167408502-[4-(Dimethylamino)phenyl]-1H-benzimidazole-6-carboxylic acid

Product 1

HCID 178482659HCID 178482659, compound

Procedure

Compound 275 was prepared according to the procedure similar to that described in Scheme V from 2-(4-dimethylaminophenyl)benzimidazole-5-carboxylic acid and 4-aminobenzhydrazide. [M+H]+ calcd for C23H22N6O2: 415.18; found: 414.91.

Sources & evidence

ORD record
ord-8f791bd18d454617b6db5b98ad3fb04a
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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