Reacción #162957

ord-9d69b0bec77c427ebf429443c5479d12

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas obtained in 95.6% yield

Procedimiento

The title compound was prepared from 3-[4-(3-phenyl-ureido)-phenyl]-isoxazole-5-carboxylic acid ethyl ester as set forth in example 8 and was obtained in 95.6% yield. Mass (ES+): 324 (M++1); IR (KBr): 3312, 1711, 1645, 1599, 1461; 1H NMR (DMSO-d6) δ: 6.97 (t, 1H), 7.28 (t, 2H), 7.45 (d, 2H), 7.59 (d, 2H), 7.71 (s, 1H), 7.87 (d, 2H), 8.76 (s, 1H), 8.96 (s, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08835428B2uspto-grants-2014_09