반응 #2155155

ord-8b712f233d5d408590ae019dfaf57094

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the reaction mixture is quenched with methanol (25 mL)
  2. 2
    농축concentrated in vacuo
  3. 3
    기타The crude material is purified by flash chromatography on silica gel (eluted with 20 to 60% EtOAc/hexanes)

실험 절차

To a solution of 1-(4-chloro-phenyl)-5-methoxymethyl-1H-pyrazole-4-carboxylic acid [(S)-1-(3-trifluoromethyl-phenyl)-butyl]-amide (510 mg, 1.1 mmol) in CH2Cl2 (10 mL) is added BBr3 (1.0 M in CH2Cl2, 1.6 mL, 1.6 mmol) dropwise. After stiffing at room temperature for 1 hour, the reaction mixture is quenched with methanol (25 mL) and concentrated in vacuo. The crude material is purified by flash chromatography on silica gel (eluted with 20 to 60% EtOAc/hexanes) to afford 1-(4-chloro-phenyl)-5-hydroxymethyl-1H-pyrazole-4-carboxylic acid [(S)-1-(3-trifluoromethyl-phenyl)-butyl]-amide (510 mg, >99%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08293917B2uspto-grants-2012_10