(2-Aminophenyl)(4,5-dimethoxy-2-methylphenyl)methanone → HCID 10187429、化合物
反応式
[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.[CH3:23][O:24][C:25]1[C:39]([O:40][CH3:41])=[CH:38][C:28]([C:29]([C:31]2[CH:37]=[CH:36][CH:35]=[CH:34][C:32]=2[NH2:33])=[O:30])=[C:27]([CH3:42])[CH:26]=1>>[CH3:23][O:24][C:25]1[C:39]([O:40][CH3:41])=[CH:38][C:28]([C:29]([C:31]2[CH:37]=[CH:36][CH:35]=[CH:34][C:32]=2[NH:33][C:20]([C:17]2[CH:16]=[CH:15][C:14]([C:3]3[CH:4]=[C:5]([C:8]4[O:9][C:10]([CH3:13])=[N:11][N:12]=4)[CH:6]=[CH:7][C:2]=3[CH3:1])=[CH:19][CH:18]=2)=[O:21])=[O:30])=[C:27]([CH3:42])[CH:26]=1参加物
3
実験手順
N-[2-(4,5-Dimethoxy-2-methylbenzoyl)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 2-(4,5-dimethoxy-2-methylbenzoyl)aniline using method I. LCMS; retention time 3.82 min, MH+ 548.
出典と根拠
- ORDレコード
- ord-e9b3f0c1d07844948d60c02099ff25ac
- 出典データセット
- uspto-grants-2008_06