Reacción #4914

Ecuación de reacción

2,4 bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide

2,3,4,5-tetrahydro-4-methyl-5-oxopyrido[3,2-f][1,4]-oxazepine-2-propanenitrile

2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide

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product

Rendimiento 24.9%

2,3,4,5-Tetrahydro-4-methyl-5-thioxopyrido[3,2-f][1,4]oxazepin-2-propanenitrile

Rendimiento 24.9%

Disolventes

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaThe reaction mixture was heated
2. 2
   Temperaturato reflux for 2 hr with vigorous mechanical stirring
3. 3
   Temperaturaheating
4. 4
   Temperaturato cool
5. 5
   workup.WAITstand overnight at room temperature
6. 6
   OtroToluene was removed by rotary evaporation (90° C., water aspirator)
7. 7
   LavadoThis was washed with 2×50 ml 2M aqueous potassium hydroxide
8. 8
   Concentraciónconcentrated by rotary evaporator (90° C., water aspirator)
9. 9
   OtroCrystallization
10. 10
    Temperaturaupon cooling
11. 11
    OtroRecrystallization from isopropyl alcohol

Procedimiento

To a solution of 11.0 g (0.04 mole) of 2,3,4,5-tetrahydro-4-methyl-5-oxopyrido[3,2-f][1,4]-oxazepine-2-propanenitrile in 175 ml toluene was added 10.5 g (0.026 mole) of 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide. The reaction mixture was heated to reflux for 2 hr with vigorous mechanical stirring. Another 3.0 g (0.007 mole) of 2,4 bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide was added and heating continued for 1 hr additional. The reaction mixture was allowed to cool and stand overnight at room temperature. Toluene was removed by rotary evaporation (90° C., water aspirator) and the residue taken up in 200 ml chloroform. This was washed with 2×50 ml 2M aqueous potassium hydroxide and concentrated by rotary evaporator (90° C., water aspirator). Crystallization ensued upon cooling. Recrystallization from isopropyl alcohol afforded 1.60 g (13.8%) product, m.p. 155°-56° C.

Fuente