تفاعل #4916

ord-969df2bb37174a8b86b8541a3ae806a4

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux for 2 hr
  2. 2
    درجة الحرارةAfter cooling
  3. 3
    ترشيحfiltered
  4. 4
    غسيلThe residue on the filter paper was washed with 50 ml of additional toluene/acetonitrile, 3/1, V/V
  5. 5
    غسيلThe filtrate was washed with 3×50 ml saturated sodium carbonate (caution: gas evolved)
  6. 6
    تجفيفdried over anhydrous sodium sulfate
  7. 7
    ترشيحfiltered
  8. 8
    workup.ADDITIONtreated with activated charcoal
  9. 9
    ترشيحfiltered again
  10. 10
    تركيزconcentrated by rotary evaporation (90° C., 30 mm)
  11. 11
    أخرىThe residual syrup was crystallized from isopropyl alcohol

الإجراء التجريبي

To 3.0 g (0.01 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methyl-1,4-oxazepino[6,7-b]-quinolin-5(4H)-one in 30 ml of acetonitrile was added 1.3 g (0.006 mole) of phosphorus pentasulfide. The mixture was stirred vigorously at reflux for 2 hr. After cooling, the reaction mixture was diluted with 60 ml of toluene and filtered. The residue on the filter paper was washed with 50 ml of additional toluene/acetonitrile, 3/1, V/V. The filtrate was washed with 3×50 ml saturated sodium carbonate (caution: gas evolved), dried over anhydrous sodium sulfate, filtered, treated with activated charcoal, filtered again and concentrated by rotary evaporation (90° C., 30 mm). The residual syrup was crystallized from isopropyl alcohol, yielding 1.6 g (52%) of yellow crystals, m.p. 114°-116° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727152uspto-grants-1988_02