Potassium Carbonate → 6-bromo-N-(2-(diethylamino)ethyl)phthalazin-1-amine
反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](Cl)=[N:7][N:6]=[CH:5]2.C(=O)([O-])[O-].[K+].[K+].[CH2:19]([N:21]([CH2:25][CH3:26])[CH2:22][CH2:23][NH2:24])[CH3:20]>CN(C)C=O.CCOC(C)=O>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([NH:24][CH2:23][CH2:22][N:21]([CH2:25][CH3:26])[CH2:19][CH3:20])=[N:7][N:6]=[CH:5]2参加物
反応条件
- 温度
- 80 °C
実験手順
6-Bromo-1-chlorophthalazine (0.22 g, 0.91 mmol) was dissolved in N,N-dimethylformamide (3 mL) and potassium carbonate (0.25 g, 1.81 mmol) and N1,N1-diethylethane-1,2-diamine (0.25 mL, 1.81 mmol) were added. The reaction mixture was heated to 80° C. for 5 h, cooled to ambient temperature and stirred for 16 h. The reaction mixture was diluted with 20 mL of EtOAc, added to an addition funnel and partitioned with sodium bicarbonate (saturated, aqueous). The organic layer was washed 3× with 20 mL of sodium bicarbonate (saturated, aqueous) and once with aqueous brine, separated, dried over sodium sulfate, and concentrated via rotovap to give crude product. The crude was purified by chromatography to obtain the title compound. Found MS (ES+): 323(M+H)+.
後処理
- temperaturecooled to ambient temperature
- additionadded to an addition funnel
- custompartitioned with sodium bicarbonate (saturated, aqueous)
- washThe organic layer was washed 3× with 20 mL of sodium bicarbonate (saturated, aqueous)
- customonce with aqueous brine, separated
- dry with materialdried over sodium sulfate
- concentrationconcentrated via rotovap
- customto give crude product
- customThe crude was purified by chromatography
出典と根拠
- ORDレコード
- ord-716d62a92dbf4913a5d22346c3782f3a
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07759337B2
反応ノート
読み込み中…