Reacción #4922

ord-66c07ea6a9ef4116951cdf9662a6bd01

Ecuación de reacción

CNC
dimethylamine
CN1CC(CCCl)Oc2ccccc2C1=O
2-(2-chloroethyl)-2,3-dihydro-4-methyl-1,4-benzoxazepin-5(4H)one
CN(C)CCC1CN(C)C(=O)c2ccccc2O1.Cl
title compound
CN(C)CCC1CN(C)C(=O)c2ccccc2O1.Cl
2-[2-(Dimethylamino)ethyl]-2,3-dihydro-4-methyl-1,4-benzoxazepin-5(4H)-one hydrochloride

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe solution was concentrated in vacuo
  2. 2
    Otrothe residue partitioned between ethyl acetate and dilute sodium hydroxide
  3. 3
    ConcentraciónThe ethyl acetate layer was concentrated
  4. 4
    workup.DISSOLUTIONthe residue comprised substantially of the free base of the title compound was dissolved in methyl isobutyl ketone-isopropanol mixture

Procedimiento

A solution of 9 g (0.2 mole) of dimethylamine in 250 ml of ethanol was added to 24 g (0.1 mole) of 2-(2-chloroethyl)-2,3-dihydro-4-methyl-1,4-benzoxazepin-5(4H)one in a steel bomb. The mixture was heated at 100° C. for 18 hrs. The solution was concentrated in vacuo and the residue partitioned between ethyl acetate and dilute sodium hydroxide. The ethyl acetate layer was concentrated and the residue comprised substantially of the free base of the title compound was dissolved in methyl isobutyl ketone-isopropanol mixture. The solution was acidified with hydrogen chloride gas to give the title compound, m.p. 188°-197° C.

Fuente

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