1,3-Dichloro-2-isothiocyanatobenzene → 2-[4-cyano-2-(2,6-dichloro-phenylamino)-3-methyl-3H-benzoimidazol-5-yl]-2-methyl-3-oxo-butyric acid ethyl ester
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[N:9]=[C:10]=S.[CH2:12]([O:14][C:15](=[O:32])[C:16]([C:21]1[CH:26]=[CH:25][C:24]([NH2:27])=[C:23]([NH:28][CH3:29])[C:22]=1[C:30]#[N:31])([CH3:20])[C:17](=[O:19])[CH3:18])[CH3:13]>C1COCC1>[CH2:12]([O:14][C:15](=[O:32])[C:16]([C:21]1[CH:26]=[CH:25][C:24]2[N:27]=[C:10]([NH:9][C:3]3[C:2]([Cl:1])=[CH:7][CH:6]=[CH:5][C:4]=3[Cl:8])[N:28]([CH3:29])[C:23]=2[C:22]=1[C:30]#[N:31])([CH3:20])[C:17](=[O:19])[CH3:18])[CH3:13]参加物
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
2,6-Dichlorophenyl isothiocyanate (3.46 g, 17.0 mmol), THF (100 mL), and 2-(4-amino-2-cyano-3-methylamino-phenyl)-2-methyl-3-oxo-butyric acid ethyl ester (4.91 g, 17.0 mmol), were added to a 250 mL round bottom flask equipped with a magnetic stir bar and the reaction was stirred at room temperature. After 2 hours, mercuric oxide (4.04 g, 18.7 mmol) was added and the reaction stirred for an additional 14 h. The resultant brown slurry was filtered through celite and washed with THF. The filtrate was concentrated and the residue triturated with diethyl ether to provide 2-[4-cyano-2-(2,6-dichloro-phenylamino)-3-methyl-3H-benzoimidazol-5-yl]-2-methyl-3-oxo-butyric acid ethyl ester (4.2 g, 54%) as a gray solid, which was used without further purification.
後処理
- customequipped with a magnetic stir bar
- stirringthe reaction stirred for an additional 14 h
- filtrationThe resultant brown slurry was filtered through celite
- washwashed with THF
- concentrationThe filtrate was concentrated
- customthe residue triturated with diethyl ether
出典と根拠
- ORDレコード
- ord-be2425312133486397c2b8d9b92db14f
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08067395B2
反応ノート
読み込み中…