反応式
C([O:5][C:6]([C:8]1[CH:9]=[C:10]([C:26]([NH:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([S:36]([CH3:39])(=[O:38])=[O:37])=[CH:32][CH:31]=2)=[O:27])[C:11](=[O:25])[N:12]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]([F:24])([F:23])[F:22])[CH:16]=2)[C:13]=1[CH3:14])=[CH2:7])CCC.C(=O)([O-])O.[Na+]>Cl>[C:6]([C:8]1[CH:9]=[C:10]([C:26]([NH:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([S:36]([CH3:39])(=[O:38])=[O:37])=[CH:32][CH:31]=2)=[O:27])[C:11](=[O:25])[N:12]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([C:21]([F:24])([F:23])[F:22])[CH:16]=2)[C:13]=1[CH3:14])(=[O:5])[CH3:7]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
Aqueous hydrochloric acid (2.0M, 50 μl) was added to a solution of 5-(1-butoxyvinyl)-6-methyl-N-[4-(methylsulfonyl)benzyl]-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2-dihydropyridine-3-carboxamide (38 mg, 67.5 μmol) in DNT (0.5 ml). After 20 min. the solution was neutralized with aqueous sodium hydrogen carbonate. The reaction mixture was purified by preparative HPLC to give the title compound as a white solid (17.6 mg, 51%).
後処理
- customThe reaction mixture was purified by preparative HPLC
出典と根拠
- ORDレコード
- ord-727b8d1c97a34d3daa701c02733a434b
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08063073B2
関連ノート
読み込み中…