HCID 28194316, compound → HCID 178482817, compound

HRID 2284221Notes

Reaction equation

HRID 2284221 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:37]=[CH:36][C:26]2[N:27]=[C:28]([NH:30][CH2:31][CH:32]([OH:35])[CH2:33][OH:34])[NH:29][C:25]=2[CH:24]=1>>[OH:35][CH:32]([CH2:33][OH:34])[CH2:31][NH:30][C:28]1[NH:27][C:26]2[CH:36]=[CH:37][C:23]([NH:22][C:14](=[O:16])[C:13]3[CH:12]=[CH:11][C:10]([NH:9][C:7](=[O:8])[C:6]4[CH:5]=[CH:4][C:3]([N:2]([CH3:1])[CH3:21])=[CH:20][CH:19]=4)=[CH:18][CH:17]=3)=[CH:24][C:25]=2[N:29]=1

Participants

3

Reactant 2

HCID 28194316HCID 28194316, compoundHCID 67112523HCID 67112523, compound

Product 1

HCID 178482817HCID 178482817, compound

Procedure

Compound 440 was prepared from 4-(4-dimethylaminobenzamido)benzoate and 5-amino-2-(2,3-dihydroxypropylamino)benzimidazole by standard conditions. [M+H]+ calcd for C26H28N6O4: 489.22; found: 489.01.

Sources & evidence

ORD record
ord-e8d7b7040d3c4b9eb81eee79d695881d
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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