Reacción #88664

ord-c57caea9a1aa46e2a14203a1113e5586

Disolventes

Condiciones de reacción

Temperatura
220°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe reaction mixture was purified by silica gel column chromatography (NH, ethyl acetate/hexane)
  2. 2
    Lavadothe obtained solid was washed with ethyl acetate

Procedimiento

A mixture of 2-(5-chloropyridin-2-yl)furo[3,2-c]pyridin-4(5H)-one (69.0 mg), 2-cyclopropyl-6-iodo-3-methylimidazo[1,2-a]pyridine (100 mg), N,N′-dimethylethylenediamine (0.030 mL), copper(I) iodide (53.3 mg), potassium carbonate (116 mg) and DMSO (3.0 mL) was heated at 220° C. for 1 hr under microwave irradiation. The reaction mixture was purified by silica gel column chromatography (NH, ethyl acetate/hexane), and the obtained solid was washed with ethyl acetate to give the title compound (2.30 mg) as a pale red solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09440987B2uspto-grants-2016_09