Réaction #659355

ord-9cc6a8df27f04689872441414797be2b

Équation de réaction

CCC(=O)c1cccnc1Cl
1-(2-Chloropyridin-3-yl)propan-1-one
Cl.NNc1ccc(OCc2ccccc2)cc1
[4-(benzyloxy)phenyl]hydrazine hydrochloride
CCc1nn(-c2ccc(OCc3ccccc3)cc2)c2ncccc12
title compound
Rendement 25.7%
CCc1nn(-c2ccc(OCc3ccccc3)cc2)c2ncccc12
1-[4-(Benzyloxy)phenyl]-3-ethyl-1H-pyrazolo[3,4-b]pyridine
Rendement 25.7%

Solvants

Conditions de réaction

Température
170°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Concentrationconcentrated
  2. 2
    AutreThe residue was purified by basic silica gel column chromatography (hexane/ethyl acetate)

Mode opératoire

1-(2-Chloropyridin-3-yl)propan-1-one (600 mg) and [4-(benzyloxy)phenyl]hydrazine hydrochloride (976 mg) were dissolved in ethanol (10 ml), and the mixture was stirred under microwave irradiation at 170° C. for 3 hr, and concentrated. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate) to give the title compound (300 mg). MS (API+): [M+H]+ 330.1.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09029388B2uspto-grants-2015_05