反応式
[NH:1]([C:3]1[N:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)[N:6]=[C:5]([NH2:15])[N:4]=1)[NH2:2].[CH2:16]([CH:23]([C:27](=O)[CH3:28])[C:24](=O)[CH3:25])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CS(C)=O.C(Cl)Cl.C(OCC)(=O)C>[CH2:16]([C:23]1[C:24]([CH3:25])=[N:2][N:1]([C:3]2[N:8]=[C:7]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=3)[N:6]=[C:5]([NH2:15])[N:4]=2)[C:27]=1[CH3:28])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 75 °C
実験手順
A suspension of 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (5.25 g, 25.6 mmol), 3-benzylpentane-2,4-dione (5.0 g, 28.4 mmol), and p-toluenesulfonic acid monohydrate (0.475 g, 2.50 mmol) in dimethylsulfoxide (50 mL) was heated to 75° C. for 20 hours. The reaction mixture was allowed to cool to room temperature, and the suspension was dissolved in methylene chloride (700 mL). The solution was washed three times with water, once with brine, dried (magnesium sulfate), and concentrated to afford a moist solid. The crude product was suspended in ethyl acetate (50 mL), heated to reflux, allowed to cool to room temperature, and filtered (repeated three times). The final product was obtained as a white solid containing 3% dimethylsulfoxide by weight: 8.63 g (90%). 1H NMR (CDCl3) δ 8.84-8.53 (m, 1H), 8.48 (d, J=7.9 Hz, 1H), 7.86-7.91 (m, 1H), 7.46-7.50 (m, 1H), 7.13-7.30 (m, 5H), 6.61 (br s, 1H), 6.40 (br s, 1H), 3.83 (s, 2H), 2.79 (s, 3H), 2.24 (s, 3H) ppm. MS (ESI) m/z 358 (M+H+).
後処理
- temperatureto cool to room temperature
- washThe solution was washed three times with water
- dry with materialonce with brine, dried (magnesium sulfate)
- concentrationconcentrated
- customto afford a moist solid
- temperatureheated
- temperatureto reflux
- temperatureto cool to room temperature
- filtrationfiltered (repeated three times)
出典と根拠
- ORDレコード
- ord-f87f65eaae3444d8a6415f0346c1362b
- 出典データセット
- uspto-grants-2005_11
- 特許番号
- US06969728B2
関連ノート
読み込み中…