Diethyl chlorophosphate → 4-[3-chloro-5-(trifluoromethyl)phenyl]-N-diethoxyphosphoryl-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine
反応式
[Cl:1][C:2]1[C:7]2OCO[C:6]=2[CH:5]=[C:4]([C:11]2[C:15]([C:16]([F:19])([F:18])[F:17])=[N:14][N:13]([C:20]3[N:25]=[CH:24][CH:23]=[CH:22][N:21]=3)[C:12]=2[NH2:26])[CH:3]=1.[H-].[Na+].[P:29](Cl)([O:34][CH2:35][CH3:36])([O:31][CH2:32][CH3:33])=[O:30]>O1CCCC1.O>[Cl:1][C:2]1[CH:3]=[C:4]([C:11]2[C:15]([C:16]([F:19])([F:18])[F:17])=[N:14][N:13]([C:20]3[N:25]=[CH:24][CH:23]=[CH:22][N:21]=3)[C:12]=2[NH:26][P:29]([O:34][CH2:35][CH3:36])([O:31][CH2:32][CH3:33])=[O:30])[CH:5]=[C:6]([C:16]([F:19])([F:18])[F:17])[CH:7]=1参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a mixture of 4-(7-chloro-1,3-benzodioxol-5-yl)-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine (0.766 g, 2.00 mmol) and NaH (0.054 g, 2.20 mmol) in tetrahydrofuran at 0° C. is added diethyl chlorophosphate (0.414 g, 2.40 mmol). The mixture is allowed to reach room temperature (20-25° C.) and further stirred for 12 hours. The reaction was diluted with water and extracted with ethyl acetate; the organic layer separated and further washed with water and then dried and concentrated. The residue was re-crystallized with a mixture of ethyl acetate and petrole ether to give the title compound (125 mg; 12%).
後処理
- customto reach room temperature
- custom(20-25° C.)
- extractionextracted with ethyl acetate
- customthe organic layer separated
- washfurther washed with water
- customdried
- concentrationconcentrated
- customThe residue was re-crystallized with a mixture of ethyl acetate and petrole ether
出典と根拠
- ORDレコード
- ord-df0409b2864a4bf3afccdb0552921cec
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09174967B2
反応ノート
読み込み中…