Реакция #4947

ord-f80487ff4d8a47d2b5d758272f0f2d59

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was heated
  2. 2
    Температураto reflux for 6.5 hr
  3. 3
    workup.WAITleft
  4. 4
    Температураheating
  5. 5
    Температураat reflux
  6. 6
    workup.WAITwas continued for 24 hr
  7. 7
    ДругоеEthanol was removed by rotary evaporation (70° C., 30 mm)
  8. 8
    Промывкаwashed with 2×50 ml dil. aqueous sodium hydroxide
  9. 9
    СушкаThe organic layer was dried over anhydrous sodium sulfate
  10. 10
    Фильтрацияfiltered
  11. 11
    Концентрированиеconcentrated by rotary evaporation (70° C., 30 mm)
  12. 12
    workup.DISSOLUTIONThe residual syrup was dissolved in isopropyl aocohol
  13. 13
    ДругоеTwo recrystallizations from isopropyl

Методика

To a suspension of 5.0 g (0.019 mole) of 2-(chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepine-5(4H)-thione in 25 ml of absolute ethanol was added 3.5 g (0.04 mole) of 2-methylpyrrolidine. The mixture was heated to reflux for 6.5 hr and left standing at room temperature overnight. Mass spec and TLC showed presence of starting materials. Approximately 5 g of potassium carbonate was added and heating at reflux was continued for 24 hr. Ethanol was removed by rotary evaporation (70° C., 30 mm). The residue was taken up in 100 ml of methylene chloride and washed with 2×50 ml dil. aqueous sodium hydroxide. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation (70° C., 30 mm). The residual syrup was dissolved in isopropyl aocohol and treated with fumaric acid affording 4.5 g (0.01 mole, 49.2%) of crude crystals. Two recrystallizations from isopropyl afforded 1.5 g (16.4%) of yellow crystals, m.p., 92°-95° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04727152uspto-grants-1988_02