반응 #155344

ord-e5fb0f73a8024e808d784f64d3c305f8

반응 방정식

[H][H]
hydrogen
COc1ccc(-c2c[nH]c3c(OCCOCc4ccccc4)ccc(F)c3c2=O)cc1
8-(2-benzyloxyethoxy)-5-fluoro-3-(4-methoxyphenyl)-1H-quinolin-4-one
COc1ccc(-c2c[nH]c3c(OCCO)ccc(F)c3c2=O)cc1
5-fluoro-8-(2-hydroxyethoxy)-3-(4-methoxyphenyl)-1H-quinolin-4-one
수율 105.3%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타After completion of the reaction
  2. 2
    기타the catalyst was removed
  3. 3
    농축the mixture was concentrated under reduced pressure
  4. 4
    기타The residue was purified
  5. 5
    농축The purified material was concentrated to dryness under reduced pressure

실험 절차

20% palladium hydroxide/carbon (5.0 g) was added to an ethanol solution (50 ml) of 8-(2-benzyloxyethoxy)-5-fluoro-3-(4-methoxyphenyl)-1H-quinolin-4-one (6.3 g, 15.0 mmol), followed by hydrogen substitution. The mixture was stirred at room temperature for 4 hours. After completion of the reaction, the catalyst was removed and the mixture was concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane:methanol=100:0→20:1). The purified material was concentrated to dryness under reduced pressure, giving a pale yellow powder of 5-fluoro-8-(2-hydroxyethoxy)-3-(4-methoxyphenyl)-1H-quinolin-4-one (5.2 g, yield: 99%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE045108E1uspto-grants-2014_09