تفاعل #155325

ord-a4491ead20674bb2860ece33ba0ea63c

معادلة التفاعل

CCCOc1cc2c(c3c(=O)c(-c4ccc(OC)cc4)cn(CCCCl)c13)CCC2
6-(3-chloropropyl)-8-(4-methoxyphenyl)-5-propoxy-1,2,3,6-tetrahydro-6-aza-cyclopenta[a]naphthalen-9-one
C1COCCN1
morpholine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
[I-].[Na+]
sodium iodide
CCCOc1cc2c(c3c(=O)c(-c4ccc(OC)cc4)cn(CCCN4CCOCC4)c13)CCC2
8-(4-methoxyphenyl)-6-(3-morpholin-4-ylpropyl)-5-propoxy-1,2,3,6-tetrahydro-6-aza-cyclopenta[a]naphthalen-9-one
المردود 38.0%

ظروف التفاعل

درجة الحرارة
60°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
    أخرىto recrystallize the residue from ethyl acetate-n-hexane

الإجراء التجريبي

A mixture containing 6-(3-chloropropyl)-8-(4-methoxyphenyl)-5-propoxy-1,2,3,6-tetrahydro-6-aza-cyclopenta[a]naphthalen-9-one (700 mg, 1.64 mmol), morpholine (165 mg, 1.90 mmol), potassium carbonate (341 mg, 2.47 mmol), sodium iodide (295 mg, 1.97 mmol) and dimethyl formamide (3 ml) was stirred at 60° C. for 7 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=70:1→50:1). The purified product was concentrated under reduced pressure to recrystallize the residue from ethyl acetate-n-hexane, giving a white powder of 8-(4-methoxyphenyl)-6-(3-morpholin-4-ylpropyl)-5-propoxy-1,2,3,6-tetrahydro-6-aza-cyclopenta[a]naphthalen-9-one (295 mg, yield: 38%).

المصدر

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