반응 #51455

ord-696a60fbc71e4c96bd637d65a3909bf4

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축the solution was concentrated
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in 100 mL of dichloromethane
  3. 3
    세척washed with sat. aq. sodium bicarbonate (50 mL)
  4. 4
    건조The organic layer was dried over sodium sulfate
  5. 5
    농축concentrated

실험 절차

To a solution of methyl 2(R/S)-(tert-butoxycarbonyl)amino-3,3-dimethyl-4-pentenoate (4.97 g, 19.3 mmol) in 50 mL of dichloromethane at 0° C. was added 16.5 mL of trifluoroacetic acid. After 2 hours, the solution was concentrated and the residue was dissolved in 100 mL of dichloromethane and washed with sat. aq. sodium bicarbonate (50 mL). The organic layer was dried over sodium sulfate and concentrated to give methyl 2(R/S)-amino-3,3-dimethyl-4-pentenoate (2.30 g), which was dissolved in 50 mL of dichloromethane and cooled to 0° C. Triethylamine (8.1 mL, 58 mmol) was added, followed by addition of 4-(4-fluorophenoxy)benzenesulfonyl chloride (6.71 g, 21.3 mmol). The reaction was allowed to warm to room temperature and stirred for 18 hours and then washed 3 N hydrochloric acid (125 mL), dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel, eluting with 20% ethyl acetate in hexane, to yield 4.41 g (61%) of methyl 2(R/S)-[4-(4-fluorophenoxy)benzenesulfonyl]amino-3,3-dimethyl4-pentenoate as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06849732B2uspto-grants-2005_02