Triethylamine → Methyl 2-(6-cyano-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-2-yl)acetate
反応式
[C:1]([C:4]1[C:5]([CH3:26])=[N:6][C:7]2[N:8]([CH:18]=[C:19]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:20]=2)[C:9]=1[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Cl:17])(=O)[NH2:2].CCN(CC)CC.FC(F)(F)C(OC(=O)C(F)(F)F)=O.[NH4+].[Cl-]>C(Cl)Cl>[C:1]([C:4]1[C:5]([CH3:26])=[N:6][C:7]2[N:8]([CH:18]=[C:19]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[N:20]=2)[C:9]=1[C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Cl:17])#[N:2]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a suspension of methyl 2-(6-carbamoyl-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-2-yl)acetate (766 mg, 1.95 mmol) in CH2Cl2 (20 mL) was added Et3N (592 mg, 5.85 mmol) and trifluoroacetic anhydride (819 mg, 3.90 mmol). The reaction mixture became a dark brown-green solution within 2 min. Satd aq NH4Cl (20 mL) was added after 30 min. The organic layer was washed with 20 mL each of satd aq NaHCO3 and water, followed by drying with MgSO4, filtration, and concentration under reduced pressure. The residue was purified by silica gel chromatography eluting product through a 40 mm i.d. by 150 mm column with 1.5% MeOH in CH2Cl2. Concentration of the fractions containing product gave methyl 2-(6-cyano-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-2-yl)acetate (583 mg, 80%) as a yellow foam.
後処理
- customwithin 2 min
- washThe organic layer was washed with 20 mL each of satd aq NaHCO3 and water
- dry with materialby drying with MgSO4, filtration, and concentration under reduced pressure
- customThe residue was purified by silica gel chromatography
- washeluting product through a 40 mm i.d
- additionConcentration of the fractions containing product
出典と根拠
- ORDレコード
- ord-5bdc80f7e0aa423cbf7b510b55469bd0
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07635699B2
反応ノート
読み込み中…