Реакция #4924

Уравнение реакции

fumaric acid

dimethylamine

ethanol

2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione

→

2-[2-(Dimethylamino)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione fumarate

Растворители

methanol

isopropyl alcohol

methylene chloride

isopropyl alcohol

Условия реакции

Обработка

1. 1
   ДругоеThe ethanol was removed in a rotary evaporator
2. 2
   Другоеleaving some water in the residue
3. 3
   Промывкаwashed with three 100 ml portions of 20% aqueous potassium carbonate solution
4. 4
   ЭкстракцияThe combined aqueous layers were extracted with three 150 ml portions of methylene chloride
5. 5
   workup.ADDITIONtreated with charcoal
6. 6
   ФильтрацияCharcoal was filtered off
7. 7
   Другоеthe filtrate was evaporated
8. 8
   Другоеto give an oil
9. 9
   Температураthe solution was heated to a slow boil
10. 10
    ДругоеCrystalline solid was obtained
11. 11
    ДругоеThe solid was recrystallized from hot 200 proof ethyl alcohol
12. 12
    ФильтрацияThe crystals were filtered off
13. 13
    Другоеtriturated in isopropyl ether at room temperature
14. 14
    Другоеagain separated
15. 15
    Фильтрацияby filtering
16. 16
    ДругоеAfter drying in a vacuum oven overnight at 85° C.
17. 17
    Другоеcrystals in the amount of 72.45 g (79%), m.p. 130°-133° C., were obtained

Методика

To a solution of 113 ml (1.0 mole) of 40% aqueous dimethylamine and 326 ml of ethanol in a steel bomb was added 48.4 g (0.189 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione. The mixture was heated at 100° C. for 14 hr. The ethanol was removed in a rotary evaporator leaving some water in the residue. The residue was dissolved in 200 ml of methylene chloride and washed with three 100 ml portions of 20% aqueous potassium carbonate solution. The combined aqueous layers were extracted with three 150 ml portions of methylene chloride. Methylene chloride solutions were combined and treated with charcoal. Charcoal was filtered off and the filtrate was evaporated to give an oil. The oil was dissolved in 215 ml isopropyl alcohol and the solution was heated to a slow boil. A solution of 21.9 g (0.19 mole) of fumaric acid in 150 ml of boiling methanol was added to the isopropyl alcohol solution. Crystalline solid was obtained weighing 63.4 g (88%). The solid was recrystallized from hot 200 proof ethyl alcohol. The crystals were filtered off and triturated in isopropyl ether at room temperature and again separated by filtering. After drying in a vacuum oven overnight at 85° C., crystals in the amount of 72.45 g (79%), m.p. 130°-133° C., were obtained.

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