تفاعل #155337

ord-441295d80dc0478abbf54a07e0db36f8

معادلة التفاعل

O=C([O-])[O-].[K+].[K+]
Potassium carbonate
Cl.ClCCN1CCOCC1
4-(2-chloroethyl)morpholine hydrochloride
CN1CCCC1=O
N-methylpyrrolidone
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)c[nH]c12
5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1 H-quinolin-4-one
CCCOc1ccc(F)c2c(=O)c(-c3ccc(OC)cc3)cn(CCN3CCOCC3)c12
5-fluoro-3-(4-methoxyphenyl)-1-(2-morpholin-4-ylethyl)-8-propoxy-1H-quinolin-4-one
المردود 75.2%

المذيبات

ظروف التفاعل

درجة الحرارة
55°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfollowed by separation
  2. 2
    غسيلThe thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution twice
  3. 3
    تركيزconcentrated under reduced pressure
  4. 4
    أخرىThe residue was purified
  5. 5
    تركيزThe purified product was concentrated under reduced pressure
  6. 6
    أخرىthe residue was recrystallized from ethyl acetate

الإجراء التجريبي

Potassium carbonate (2.1 g, 15.2 mmol) and 4-(2-chloroethyl)morpholine hydrochloride (1.36 g, 7.31 mmol) were added to an N-methylpyrrolidone (NMP) solution (5 ml) of 5-fluoro-3-(4-methoxyphenyl)-8-propoxy-1 H-quinolin-4-one (1.0 g, 3.05 mmol) and then stirred at 50 to 60° C. for 45 hours. Water and ethyl acetate were added to the reaction mixture, followed by separation. The thus-obtained organic layer was washed with an aqueous saturated sodium chloride solution twice, and then concentrated under reduced pressure. The residue was purified using silica gel column chromatography (dichloromethane:methanol=50:1→30:1). The purified product was concentrated under reduced pressure, and the residue was recrystallized from ethyl acetate, giving a white powder of 5-fluoro-3-(4-methoxyphenyl)-1-(2-morpholin-4-ylethyl)-8-propoxy-1H-quinolin-4-one (1.01 g, yield: 75%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE045108E1uspto-grants-2014_09