Reacción #4299

ord-d69cadb84c1f457aa9645d6fe5e18d9e

Ecuación de reacción

Cl.Cl.Nc1c(F)c(N)c(F)c(F)c1F
dihydrochloride
CC(C)N(CCN1C(=O)c2ccccc2C1=O)C(C)C
2-[[N,N-bis(1-methylethyl)amino]ethyl]-2H-isoindole-1,3-dione
NN.O
hydrazine hydrate
CC(C)N(CCN)C(C)C.Cl.Cl
N,N-bis(1-Methylethyl)-1,2-ethanediamine, dihydrochloride

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 5 hours
  2. 2
    OtroA white solid formed
  3. 3
    ConcentraciónThe reaction mixture was concentrated almost to dryness on the rotary evaporator
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in chloroform
  5. 5
    Extracciónextracted with 10% sodium hydroxide
  6. 6
    OtroAfter removing chloroform
  7. 7
    Otroa brown oil was obtained
  8. 8
    OtroAfter recrystallization from methanol-diethyl ether, 1.50 g (20%) of white crystalline product
  9. 9
    Otrom.p. 178°-182° C. (decomposition) was obtained

Procedimiento

A solution of 40.54 g (0.148 mole) of 2-[2-[[N,N-bis(1-methylethyl)amino]ethyl]-2H-isoindole-1,3-dione and hydrazine hydrate (85%, 11.8 g, 0.2 mole) in 400 ml of 95% ethanol was heated at reflux for 5 hours. The reaction mixture was allowed to cool to room temperature while standing overnight. A white solid formed. The reaction mixture was concentrated almost to dryness on the rotary evaporator. The residue was dissolved in chloroform and extracted with 10% sodium hydroxide. After removing chloroform, a brown oil was obtained. A portion of the oil was dissolved in methanol and converted to the dihydrochloride salt. After recrystallization from methanol-diethyl ether, 1.50 g (20%) of white crystalline product, m.p. 178°-182° C. (decomposition) was obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04724235uspto-grants-1988_02