(Diethylamino)sulfur trifluoride → 2-Chloro-4-(1-fluoroethyl)pyrimidine
反応式
[Cl:1][C:2]1[N:7]=[C:6]([CH:8](O)[CH3:9])[CH:5]=[CH:4][N:3]=1.C(N(S(F)(F)[F:17])CC)C>ClCCl>[Cl:1][C:2]1[N:7]=[C:6]([CH:8]([F:17])[CH3:9])[CH:5]=[CH:4][N:3]=1参加物
4
実験手順
To a solution of 1-(2-chloropyrimidin-4-yl)ethanol (150 mg, 0.950 mmol) in dichloromethane (3 mL) at 0° C. was added diethylaminosulfur trifluoride (183 mg, 1.14 mmol) dropwise and stirred for 3 hr. The solution was diluted with dichloromethane, washed with saturated aqueous NaHCO3, dried with MgSO4, and concentrated to dryness. Purification on silica gel by flash chromatography (0-50% EtOAc/hexanes) afforded 2-chloro-4-(1-fluoroethyl)pyrimidine (75 mg, 0.467 mmol, 49% yield) as a yellow oil. MS ESI: [M+H]+ m/z 161.0. 1H NMR (500 MHz, CDCl3) δ 8.67 (d, J=4.2, 1H), 7.46 (d, J=4.2, 1H), 5.58 (dq, J=6.7, 48, 1H), 1.74-1.57 (m, 3H).
後処理
- washwashed with saturated aqueous NaHCO3
- dry with materialdried with MgSO4
- concentrationconcentrated to dryness
- customPurification on silica gel by flash chromatography (0-50% EtOAc/hexanes)
出典と根拠
- ORDレコード
- ord-28e7fc473eff4192977d310059266b77
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08759366B2
反応ノート
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