Reacción #4909

ord-2835159553ab4fcdb331894bd71cc090

Ecuación de reacción

CN1CC(CCCl)Sc2ncccc2C1=O
2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]thiazepin-5(4H)-one
COc1ccc(P2(=S)SP(=S)(c3ccc(OC)cc3)S2)cc1
2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide
CN1CC(CCCl)Sc2ncccc2C1=S
2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-thiazepine-5(4H)-thione

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas refluxed for 3 hr
  2. 2
    Extracciónextracted twice with dilute sodium hydroxide
  3. 3
    ConcentraciónThe organic layer was concentrated
  4. 4
    Otrothe residue chromatographed on the high pressure liquid chromatograph

Procedimiento

A mixture of 4.3 g (0.017 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f][1,4]thiazepin-5(4H)-one, 100 ml of toluene and 4.8 g (0.012 mole) of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide was refluxed for 3 hr and then extracted twice with dilute sodium hydroxide. The organic layer was concentrated and the residue chromatographed on the high pressure liquid chromatograph using a silica column and 50% ethyl acetate-50% hexane. The yield of title compound was 2 g, m.p. 160°-162° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04727152uspto-grants-1988_02