反応式
[CH2:1]([N:3]([C:20](=[O:24])[CH:21]([CH3:23])[CH3:22])[C:4]1[CH:5]=[C:6]([C:17](O)=[O:18])[CH:7]=[C:8]([C:10]2[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][CH:11]=2)[CH:9]=1)[CH3:2].[N:25]1[CH:30]=[CH:29][N:28]=[CH:27][C:26]=1[CH:31]([NH2:33])[CH3:32]>>[N:25]1[CH:30]=[CH:29][N:28]=[CH:27][C:26]=1[CH:31]([NH:33][C:17]([C:6]1[CH:7]=[C:8]([C:10]2[CH:11]=[CH:12][C:13]([CH3:16])=[CH:14][CH:15]=2)[CH:9]=[C:4]([N:3]([CH2:1][CH3:2])[C:20](=[O:24])[CH:21]([CH3:22])[CH3:23])[CH:5]=1)=[O:18])[CH3:32]参加物
3
実験手順
5-(Ethyl-isobutyryl-amino)-4′-methyl-biphenyl-3-carboxylic acid was reacted with 1-pyrazin-2-yl-ethylamine following the procedure of step 5 of Example 1 to give 5-(ethyl-isobutyryl-amino)-4′-methyl-biphenyl-3-carboxylic acid (1-pyrazin-2-yl-ethyl)-amide, MS (M+H)=431.
出典と根拠
- ORDレコード
- ord-9fba1917b4d747b5a0294e36635bb50f
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08895589B2
関連ノート
読み込み中…