3-Amino-N-methylbenzamide → HCID 25093463, compound

HRID 131716

Reaction equation

HRID 131716 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]([CH3:13])=[N:11][N:12]=2)=[CH:4][C:3]=1[C:14]1[CH:19]=[CH:18][C:17]([C:20]([OH:22])=O)=[CH:16][CH:15]=1.[CH3:23][NH:24][C:25](=[O:33])[C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([NH2:32])[CH:27]=1>>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]([CH3:13])=[N:11][N:12]=2)=[CH:4][C:3]=1[C:14]1[CH:15]=[CH:16][C:17]([C:20]([NH:32][C:28]2[CH:29]=[CH:30][CH:31]=[C:26]([C:25]([NH:24][CH3:23])=[O:33])[CH:27]=2)=[O:22])=[CH:18][CH:19]=1

Participants

3

Reactant 2

HCID 6765263-Amino-N-methylbenzamideHCID 112201194-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic Acid

Product 1

HCID 25093463HCID 25093463, compound

Procedure

2′-Methyl-N-{3-[(methylamino)carbonyl]phenyl}-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxamide was prepared from 2′-methyl-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-1,1′-biphenyl-4-carboxylic acid and N-methyl-3-aminobenzamide using method I. LCMS; retention time 3.04 min, MH+ 427.

Sources & evidence

ORD record
ord-42d9af76fad44371a6734f725e791661
Source dataset
uspto-grants-2008_06
Patent number
US07384963B2

Linked notes

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