4-(Dimethylamino)benzoic acid → HCID 178482815, compound

HRID 2284105Notes

Reaction equation

HRID 2284105 reaction equation
[CH3:1][N:2]([CH3:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][CH:4]=1.[NH2:13][C:14]1[CH:29]=[CH:28][C:17]2[N:18]=[C:19]([NH:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[NH:20][C:16]=2[CH:15]=1>>[CH3:12][N:2]([CH3:1])[C:3]1[CH:4]=[CH:5][C:6]([C:7]([NH:13][C:14]2[CH:29]=[CH:28][C:17]3[NH:18][C:19]([NH:21][C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)=[N:20][C:16]=3[CH:15]=2)=[O:9])=[CH:10][CH:11]=1

Participants

3

Reactant 2

HCID 120924-(Dimethylamino)benzoic acidHCID 53900383HCID 53900383, compound

Product 1

HCID 178482815HCID 178482815, compound

Procedure

Compound 180 was prepared according to the procedure similar to that described in Scheme III from 4-dimethylaminobenzoic acid and 5-amino-2-phenylaminobenzimidazole. [M+H]+ calcd for C22H22N5O: 372.18; found: 371.95.

Sources & evidence

ORD record
ord-ed7fed064064459e8dbc617a22df56ea
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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