Benzoate → HCID 178521793, compound

HRID 2284246Notes

Reaction equation

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

Participants

Reactant 2

HCID 242Benzoate

HCID 178507342HCID 178507342, compound

Product 1

HCID 178521793HCID 178521793, compound

Procedure

Compound 479 was prepared from 5-amino-2-(4-(pyridin-2-yl)phenyl)-1H-benzimidazole and benzoate by standard conditions. [M+H]+ calcd for C25H18N4O: 391.16; found: 390.91.

Sources & evidence

ORD record: ord-0d77c8081d754d00a57666df7f3a0ad5
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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