Reaktion #45094

ord-f3403cefc69c4b158649f4ab3d6f009a

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe crude product was purified by ion exchange chromatography
  2. 2
    WaschenThe desired product was eluted from the column
  3. 3
    Sonstigeto afford impure material
  4. 4
    SonstigeThe concentrated eluent was purified by preparative HPLC
  5. 5
    workup.ADDITIONFractions containing the desired compound
  6. 6
    Sonstigewere evaporated to dryness

Vorschrift

(2S,6R)-2,6-Dimethylpiperazine (228 mg, 2.00 mmol) was added in one portion to 5-chloro-N-[5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-yl]pyrazine-2-carboxamide (388 mg, 1.00 mmol) in anhydrous dimethylsulfoxide (1.00 ml) at 25° C. The resulting solution was stirred at 100° C. for 18 h. The crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH to afford impure material. The concentrated eluent was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford the title compound (164 mg, 35%) as a cream solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737149B2uspto-grants-2010_06