Trifluoroacetic acid → 3-Chloro-2-(3,3-difluorocyclobutyl)pyridine
反応式
[Cl:1][C:2]1[C:3]([C:8]2(C(OC(C)(C)C)=O)[CH2:11][C:10]([F:13])([F:12])[CH2:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1.C(O)(C(F)(F)F)=O>C(Cl)Cl>[Cl:1][C:2]1[C:3]([CH:8]2[CH2:9][C:10]([F:13])([F:12])[CH2:11]2)=[N:4][CH:5]=[CH:6][CH:7]=1参加物
反応条件
- 温度
- 90 °C
実験手順
To a solution of tert-butyl 1-(3-chloropyridin-2-yl)-3,3-difluorocyclobutanecarboxylate (Preparation 229, 500 mg, 1.65 mmol) in DCM (6.5 mL) was added TFA (0.50 mL, 6.6 mmol) at room temperature under N2. The resulting solution was stirred for 18 hours. The solvent was removed in vacuo and toluene (5 mL) was added. The resulting mixture was warmed up to 90° C. and stirred for 18 hours. The reaction mixture was cooled to room temperature and diluted with EtOAc and water. The organic phase was washed with saturated aqueous NaHCO3 solution, then brine, dried over Na2SO4, filtered, and concentrated in vacuo to give the crude product as a dark brown oil. The crude product was purified by silica gel column chromatography eluting with 0-30% EtOAc in heptane to give the title compound (271 mg, 81%) as a colourless oil.
後処理
- customThe solvent was removed in vacuo and toluene (5 mL)
- additionwas added
- stirringstirred for 18 hours
- temperatureThe reaction mixture was cooled to room temperature
- additiondiluted with EtOAc and water
- washThe organic phase was washed with saturated aqueous NaHCO3 solution
- dry with materialbrine, dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give the crude product as a dark brown oil
- customThe crude product was purified by silica gel column chromatography
- washeluting with 0-30% EtOAc in heptane
出典と根拠
- ORDレコード
- ord-626c33b2ef1c48c3a312b3cf766fc797
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08592629B2
反応ノート
読み込み中…