反応 #1563931

ord-3e4850fa9c2442fc89d428e045d0511a

反応方程式

Cl
HCl
CC(C)(C)[S@](=O)N1CCC[C@@H]1c1cc(F)ccc1F
(R)-1-((S)-tert-butylsulfinyl)-2-(2,5-difluorophenyl)pyrrolidine
Cl.Fc1ccc(F)c([C@H]2CCCN2)c1
title compound
Cl.Fc1ccc(F)c([C@H]2CCCN2)c1
(R)-2-(2,5-difluorophenyl)pyrrolidine Hydrochloride

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮After which the reaction mixture was concentrated under reduced pressure
  2. 2
    その他to afford the crude product
  3. 3
    その他The crude product was purified
  4. 4
    洗浄by washing with diethyl ether

実験手順

4M HCl solution (in Dioxane) (75 mL) was added to stirred solution of (R)-1-((S)-tert-butylsulfinyl)-2-(2,5-difluorophenyl)pyrrolidine (15 g, 52.19 mmol) in Dioxane (25 mL) and stirring was continued at 20-35° C. for 4 h. After which the reaction mixture was concentrated under reduced pressure to afford the crude product. The crude product was purified by washing with diethyl ether to afford 7.5 g of the title compound as a white solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09402833B2uspto-grants-2016_08