Trifluoroacetic acid → 3-Chloro-2-(3,3-difluorocyclobutyl)pyridine

HRID 2048093ノート

反応式

HRID 2048093 の反応式
[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

4

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

  1. customThe solvent was removed in vacuo and toluene (5 mL)
  2. additionwas added
  3. stirringstirred for 18 hours
  4. temperatureThe reaction mixture was cooled to room temperature
  5. additiondiluted with EtOAc and water
  6. washThe organic phase was washed with saturated aqueous NaHCO3 solution
  7. dry with materialbrine, dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customto give the crude product as a dark brown oil
  11. customThe crude product was purified by silica gel column chromatography
  12. 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

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