Benzimidazole-5-carboxylate → HCID 178482819, compound

Reaction equation

[CH3:1][N:2]([CH3:19])[C:3]1[CH:18]=[CH:17][C:6]([C:7]([NH:9][C:10]2[CH:16]=[CH:15][C:13]([NH2:14])=[CH:12][CH:11]=2)=[O:8])=[CH:5][CH:4]=1.[N:20]1[C:24]2[CH:25]=[CH:26][C:27]([C:29]([O-])=[O:30])=[CH:28][C:23]=2[NH:22][CH:21]=1>>[CH3:1][N:2]([CH3:19])[C:3]1[CH:4]=[CH:5][C:6]([C:7]([NH:9][C:10]2[CH:16]=[CH:15][C:13]([NH:14][C:29]([C:27]3[CH:26]=[CH:25][C:24]4[NH:20][CH:21]=[N:22][C:23]=4[CH:28]=3)=[O:30])=[CH:12][CH:11]=2)=[O:8])=[CH:17][CH:18]=1

Participants

Reactant 2

HCID 3580685Benzimidazole-5-carboxylate

HCID 123899444-(4-Dimethylaminobenzamido)aniline

Product 1

HCID 178482819HCID 178482819, compound

Procedure

Compound 445 was prepared from 4-(4-dimethylaminobenzamido)aniline and benzimidazole-5-carboxylate by standard conditions. [M+H]+ calcd for C23H21N5O2: 400.17; found: 400.01.

Sources & evidence

ORD record: ord-2dcaaf9de03741a385f2e5ae5d820c7a
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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