Реакция #2671

ord-0a483aea8a4b498cbaefafb7e4383a84

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe residue was chromatographed on silica
  2. 2
    Промывкаeluting with a dichloromethane-methanol (95-5) mixture

Методика

0.640 g of the product of Step D and and 0.474 g of oxo-[2-[(triphenylmethyl)-amino]-thiazol-4-yl]-acetic acid (Belgian Patent Application No. 864,828) were stirred for 4 and a half hours under nitrogen and at ambient temperature in the presence of 20 ml of methanol. Then, the solvent was eliminated, and the residue was chromatographed on silica, eluting with a dichloromethane-methanol (95-5) mixture to obtain 0.612 g of the expected product with a Rf=0.35 [eluant: dichloromethane-methanol (9-1)].

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05728828uspto-grants-1998_03