Sodium hydride → HCID 86704207、化合物
反応式
[N+:1]([C:4]1[CH:5]=[N:6][N:7]([CH2:9][CH2:10][OH:11])[CH:8]=1)([O-:3])=[O:2].[H-].[Na+].Cl[C:15]1[N:20]=[C:19]([O:21][CH3:22])[CH:18]=[C:17]([O:23][CH3:24])[N:16]=1>C1COCC1>[CH3:24][O:23][C:17]1[CH:18]=[C:19]([O:21][CH3:22])[N:20]=[C:15]([O:11][CH2:10][CH2:9][N:7]2[CH:8]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=[N:6]2)[N:16]=1参加物
反応条件
- 温度
- 0 °C
実験手順
To an ice-cooled solution of 2-(4-nitro-1H-pyrazol-1-yl)ethanol (1.90 g, 12.02 mmol) in THF (60 mL), NaH (673 mg, 16.82 mmol, 60%) was added and the solution was stirred for 5 min at 0° C., then the ice bath was removed and the reaction mixture was stirred at rt for 30 min, before 2-chloro-4,6-dimethoxypyrimidine (2.31 g, 13.22 mmol) was added. After 40 min at rt, the reaction mixture was quenched with water and the org. solvent was removed in vacuo. The aq. layer was extracted with DCM (1×), then acidified with 1 N HCl-solution to pH 2, and extracted with DCM (2×). The combined org. layers were washed with brine, dried (MgSO4), filtered and the solvent removed under reduced pressure. Purification by crystallization (DCM-hept-mixture) yielded 4,6-dimethoxy-2-(2-(4-nitro-1H-pyrazol-1-yl)ethoxy)pyrimidine as a beige solid. LC-MS conditions A: tR=0.88 min, [M+H]+=295.98.
後処理
- additionwas added
- customthe ice bath was removed
- additionwas added
- waitAfter 40 min at rt
- customthe reaction mixture was quenched with water
- customsolvent was removed in vacuo
- extractionThe aq. layer was extracted with DCM (1×)
- extractionextracted with DCM (2×)
- washlayers were washed with brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- customthe solvent removed under reduced pressure
- customPurification
- customby crystallization (DCM-hept-mixture)
出典と根拠
- ORDレコード
- ord-832a44f153694ebd9fc1c6d75eccc172
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09303023B2
反応ノート
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