Reaktion #88422

ord-231a675529f54196a2a67c83afa3c030

Reaktionsbedingungen

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

Aufarbeitung

  1. 1
    Sonstigeobtained in (Example 1.4) <Step 1>
  2. 2
    ExtraktionAfter extraction of organic layers, water layers
  3. 3
    Extraktionwere extracted with ethyl acetate (50 ml)
  4. 4
    WaschenThe combined organic layer was washed with a saturated saline
  5. 5
    Trocknenwas then dried over anhydrous sodium sulfate
  6. 6
    workup.DISTILLATIONThe solvent was distilled away under reduced pressure
  7. 7
    Sonstigethe obtained residue was then purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=93:7-40:60)

Vorschrift

Cyclopropylboronic acid (61 mg), palladium acetate (11 mg), phosphoric acid potassium salts (203 mg), water (0.53 ml), and tricyclohexylphosphine (27 mg) were added to a toluene (6 ml) solution of the methyl 4-(5-bromo-4-(difluoromethyl)thiazol-2-yl)-1-methyl-1H-pyrazole-5-carboxylate (84 mg) obtained in (Example 1.4) <Step 1>, and the obtained mixture was then stirred in a nitrogen atmosphere at 100° C. for 1.5 hours. Thereafter, ethyl acetate (50 ml) and a saturated sodium hydrogen carbonate aqueous solution (30 ml) were added to the reaction solution. After extraction of organic layers, water layers were extracted with ethyl acetate (50 ml). The organic layers were combined. The combined organic layer was washed with a saturated saline, and was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure, and the obtained residue was then purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=93:7-40:60), so as to obtain the title compound (62 mg) in the form of a light brown solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09440970B2uspto-grants-2016_09