반응 #836853

ord-77a9a079cf8649368ebeaed1800b486f

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축the solution was concentrated
  2. 2
    기타The product was triturated with diethyl ether

실험 절차

In an analogous manner to Example 135, step 4 1-[1-(2′-fluoro-1,1′-biphenyl-3-yl)-2-piperazin-1-ylethyl]cyclohexanol dihydrochloride was prepared from tert-butyl 4-[2-(2′-fluoro-biphenyl-3-yl)-2-(1-hydroxycyclohexyl)ethyl]piperazine-1-carboxylate. The compound was neutralized with 10% aqueous potassium carbonate, and the residue dissolved in methanol. One equivalent of maleic acid was then added and the solution was concentrated. The product was triturated with diethyl ether to yield 1-[1-(2′-fluoro-1,1′-biphenyl-3-yl)-2-piperazin-1-ylethyl]cyclohexanol maleate as a colorless solid. MS (ESI) m/z 383 ([M+H]+); Anal. Calcd for C24H31FN2O.C4H4O4.0.50H2O: C, 66.25; H, 7.15; N, 5.52. Found: C, 66.03; H, 7.38; N, 5.31.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07402698B2uspto-grants-2008_07