Reaktion #937121

ord-d83f0ac1f0c9476f859ad6f92b7614fa

Lösungsmittel

Reaktionsbedingungen

Temperatur
130°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter completion of the reaction
  2. 2
    Extraktionfollowed by extraction with ethyl acetate
  3. 3
    WaschenThe organic layer was washed with saturated sodium chloride solution
  4. 4
    Trocknendried with anhydrous magnesium sulfate
  5. 5
    Einengenconcentrated

Vorschrift

A mixture of 0.12 g of 3-(5-amino-4-fluorophenyl)-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazine (present compound 1-19) and 0.23 g of ethyl 2-bromopropionate was stirred at 130° C. for 3 hours. After completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography, which afforded 52 mg (yield, 32%) of 3-{5-[1-(ethoxycarbonyl)ethylamino]-4-fluorophenyl}-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazine (present compound 1-355; m.p., 78.2° C.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06015774uspto-grants-2000_01