Reacción #1869222

ord-1e603eb5cd654201b6b599f477ad620a

Ecuación de reacción

CCN1C(=O)C(C(=O)OC)C(=O)c2cc(Br)cc(C)c21
methyl 6-bromo-1-ethyl-8-methyl-4-oxo-1,4-dihydroquinolone-3-carboxylate
Cc1cccnc1N
2-amino-3-methylpyridine
CC1(C)c2cccc(P(c3ccccc3)c3ccccc3)c2Oc2c(P(c3ccccc3)c3ccccc3)cccc21
XANTPHOS
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCN1C(=O)C(C(=O)OC)C(=O)c2cc(Nc3ncccc3C)cc(C)c21
Methyl 1-ethyl-8-methyl-6-(3-methylpyridin-2-ylamino)-4-oxo-1,4-dihydroquinolone-3-carboxylate

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwere added
  2. 2
    OtroThe pure product was isolated from the reaction solution by chromatography on an HPLC system
  3. 3
    Otrorose to 95% over the course of 20 minutes

Procedimiento

100 mg of methyl 6-bromo-1-ethyl-8-methyl-4-oxo-1,4-dihydroquinolone-3-carboxylate were transferred together with 40 mg of 2-amino-3-methylpyridine, 20 mg of Pd(OAc)2, 60 mg of XANTPHOS and 250 mg of cesium carbonate into a suitable reaction vessel, a protective gas atmosphere was generated with argon, and 10 ml of dioxane were added. The mixture was then heated at 80° C. for 8 h. The pure product was isolated from the reaction solution by chromatography on an HPLC system. This entailed use of a Merck Purospher RP-18 column and an acetonitrile:water mixture as eluent; the initial acetonitrile content was 15% and rose to 95% over the course of 20 minutes.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07498341B2uspto-grants-2009_03