Water → 3-((2-Chloropyridin-4-yl)oxy)-2-methyl-6-nitropyridine
反応式
Br[C:2]1[C:3]([CH3:11])=[N:4][C:5]([N+:8]([O-:10])=[O:9])=[CH:6][CH:7]=1.C([O-])([O-])=O.[K+].[K+].[Cl:18][C:19]1[CH:24]=[C:23]([OH:25])[CH:22]=[CH:21][N:20]=1.O>CN(C=O)C.CCOC(C)=O>[Cl:18][C:19]1[CH:24]=[C:23]([O:25][C:2]2[C:3]([CH3:11])=[N:4][C:5]([N+:8]([O-:10])=[O:9])=[CH:6][CH:7]=2)[CH:22]=[CH:21][N:20]=1参加物
反応条件
- 温度
- 100 °C
実験手順
A solution of 3-bromo-2-methyl-6-nitropyridine (25.59 g, 118 mmol), K2CO3 (48.9 g, 354 mmol) and 2-chloro-4-hydroxy-pyridine (30.6 g, 236 mmol) in DMF (160 mL) was sparged with Ar, heated at 100° C. overnight, then cooled to RT. The mixture was treated with water and EtOAc, the solids removed via filtration through diatomaceous earth and washed with water, EtOAc, then DCM. The aqueous filtrate was extracted with EtOAc (2×) and the organic extracts were combined with the organic filtrates, washed with water, then brine, dried over Na2SO4 and concentrated to dryness. The residue was treated with MTBE, sonicated and the resulting solid collected via filtration to afford 3-((2-chloropyridin-4-yl)oxy)-2-methyl-6-nitropyridine (17.16 g, 55%). 1H NMR (400 MHz, DMSO-d6): δ 8.38 (d, J=5.7 Hz, 1 H), 8.25 (d, J=8.7 Hz, 1 H), 7.95 (d, J=8.7 Hz, 1 H), 7.29 (d, J=2.3 Hz, 1 H), 7.16 (dd, J=5.7, 2.3 Hz, 1 H), 2.46 (s, 3 H); MS (ESI) m/z: 266.0 (M+H+).
後処理
- temperaturecooled to RT
- customthe solids removed via filtration through diatomaceous earth
- washwashed with water, EtOAc
- extractionThe aqueous filtrate was extracted with EtOAc (2×)
- washwashed with water
- dry with materialbrine, dried over Na2SO4
- concentrationconcentrated to dryness
- additionThe residue was treated with MTBE
- customsonicated
- filtrationthe resulting solid collected via filtration
出典と根拠
- ORDレコード
- ord-62f516bb86294c7980d0a253d703cb01
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09133183B2
反応ノート
読み込み中…