반응 #49811

ord-cc4af762ad524c07840cce09b6104c77

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과the catalyst was filtered off with suction
  2. 2
    농축the filtrate was concentrated
  3. 3
    기타chromatographed on silica gel (ethyl acetate/heptane=1:2)

실험 절차

Methyl N-(6-chloro-3-nitro-2-pyridyl)-2-aminoisobutyrate (4.0 g, 14.6 mmol) was hydrogenated in 250 ml of methanol with Raney nickel catalysis under 1 atm of hydrogen. After hydrogen uptake ceased, the catalyst was filtered off with suction, and the filtrate was concentrated and chromatographed on silica gel (ethyl acetate/heptane=1:2). 1.89 g (61%) of the compound of Example 15, of melting point 229° C., were obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05424311uspto-grants-1995_06