TCMDC-123859 → HCID 178482816, compound

HRID 2284222Notes

Reaction equation

HRID 2284222 reaction equation
[CH3:1][N:2]([CH3:21])[C:3]1[CH:20]=[CH:19][C:6]([C:7]([NH:9][C:10]2[CH:18]=[CH:17][C:13]([C:14]([O-:16])=O)=[CH:12][CH:11]=2)=[O:8])=[CH:5][CH:4]=1.[NH2:22][C:23]1[CH:40]=[CH:39][C:26]2[N:27]=[C:28]([C:30]3[CH:35]=[CH:34][C:33]([N:36]([CH3:38])[CH3:37])=[CH:32][CH:31]=3)[NH:29][C:25]=2[CH:24]=1>>[CH3:37][N:36]([CH3:38])[C:33]1[CH:32]=[CH:31][C:30]([C:28]2[NH:27][C:26]3[CH:39]=[CH:40][C:23]([NH:22][C:14](=[O:16])[C:13]4[CH:12]=[CH:11][C:10]([NH:9][C:7](=[O:8])[C:6]5[CH:5]=[CH:4][C:3]([N:2]([CH3:1])[CH3:21])=[CH:20][CH:19]=5)=[CH:18][CH:17]=4)=[CH:24][C:25]=3[N:29]=2)=[CH:35][CH:34]=1

Participants

3

Reactant 2

HCID 763219TCMDC-123859HCID 28194316HCID 28194316, compound

Product 1

HCID 178482816HCID 178482816, compound

Procedure

Compound 442 was prepared from 4-(4-dimethylaminobenzamido)benzoate and 5-amino-2-(4-dimethylaminophenyl)benzimidazole by standard conditions. [M+H]+ calcd for C31H30N6O2: 519.24; found: 518.99.

Sources & evidence

ORD record
ord-aa651a45efb2466599dafc118ad11730
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

Loading…