P-Phenylenediamine → HCID 136352332, compound

HRID 2284171Notes

Reaction equation

HRID 2284171 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](O)=[O:19])[CH:15]=[CH:14][C:12]=3[N:13]=2)=[CH:5][CH:4]=1.[C:22]1([NH2:29])[CH:27]=[CH:26][C:25]([NH2:28])=[CH:24][CH:23]=1>>[C:22]1([NH:29][C:18]([C:16]2[CH:15]=[CH:14][C:12]3[NH:13][C:9]([C:6]4[CH:5]=[CH:4][C:3]([N:2]([CH3:21])[CH3:1])=[CH:8][CH:7]=4)=[N:10][C:11]=3[CH:17]=2)=[O:19])[CH:27]=[CH:26][C:25]([NH:28][C:18]([C:16]2[CH:15]=[CH:14][C:12]3[NH:13][C:9]([C:6]4[CH:5]=[CH:4][C:3]([N:2]([CH3:21])[CH3:1])=[CH:8][CH:7]=4)=[N:10][C:11]=3[CH:17]=2)=[O:19])=[CH:24][CH:23]=1

Participants

3

Procedure

Compound 283 was prepared according to the procedure similar to that described in Scheme V from 2-(4-dimethylaminophenyl)benzimidazole-5-carboxylic acid and 1,4-phenylenediamine. [M+H]+ calcd for C38H34N8O2: 635.28; found: 635.05.

Sources & evidence

ORD record
ord-322bcfc2ebc64382ac612d39604ab4a9
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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