4-[2-methyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)phenyl]benzoic Acid → HCID 10142660, compound
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](O)=[O:21])=[CH:16][CH:15]=1.C(N[C:27]1[CH:40]=[CH:39][CH:38]=[CH:37][C:28]=1[O:29][C:30]1[CH:36]=[CH:35][C:33]([NH2:34])=[CH:32][CH:31]=1)(=O)C>>[C:8]([NH:12][C:39]1[CH:40]=[CH:27][C:28]([O:29][C:30]2[CH:31]=[CH:32][C:33]([NH:34][C:20]([C:17]3[CH:18]=[CH:19][C:14]([C:3]4[CH:4]=[C:5]([C:8]5[O:9][C:10]([CH3:13])=[N:11][N:12]=5)[CH:6]=[CH:7][C:2]=4[CH3:1])=[CH:15][CH:16]=3)=[O:21])=[CH:35][CH:36]=2)=[CH:37][CH:38]=1)(=[O:9])[CH3:5]Participants
3
Procedure
N-[4-(4-Acetylaminophenoxy)phenyl]-2′-methyl-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 4-(acetylaminophenoxy)aniline using method I. LCMS; retention time 3.42 min, MH+ 519.
Sources & evidence
- ORD record
- ord-8e7551d6d09b491cb24f8cbf2a1daa85
- Source dataset
- uspto-grants-2008_06
- Patent number
- US07384963B2
Reaction notes
Loading…