반응 #1869195

ord-22eb2861c23d43d680bdd14f2f88c5d2

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타prepared
  2. 2
    여과was filtered through Celite®
  3. 3
    농축The filtrate was concentrated under reduced pressure
  4. 4
    기타the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3)

실험 절차

To a solution of the enantiomeric mixture of cis-4-benzylamino-1-tert-butoxycarbonyl-3-fluoropiperidine (prepared according to the procedures of J. Med. Chem. 1999, 42, 2087-2104, 1.0 g, 3.2 mmole) in EtOH (40 mL) was added 3 N HCl (2.5 L) and 10% Pd/C (50 mg). The reaction was shaken under H2 (40 psi) on a Parr apparatus for 14 h, then was filtered through Celite®. The filtrate was concentrated under reduced pressure, and the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3) to afford the title compound (370 mg, 53%) as a white solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07498326B2uspto-grants-2009_03