Réaction #65566

ord-ad69d7ccdf8a44a18f874ef8d8f28ce9

Équation de réaction

CCCN=C=O
propyl isocyanate
COC(=O)C(CN)c1cccc2ccccc12.Cl
2-(1-naphthyl)-2-(methoxycarbonyl)ethylamine hydrochloride
Cl
hydrochloric acid
CCCNC(=O)NCC(C(=O)OC)c1cccc2ccccc12
N-[2-(1-naphthyl)-2-(methoxycarbonyl)ethyl]-N'-propylurea

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONpoured into ice-cold water
  2. 2
    AutreThe precipitate formed
  3. 3
    Lavagewashed with water
  4. 4
    Autredried
  5. 5
    Autrerecrystallized in a toluene/cyclohexane mixture

Mode opératoire

0.011 mol of propyl isocyanate is added dropwise and with magnetic stirring to a suspension of 0.01 mol of 2-(1-naphthyl)-2-(methoxycarbonyl)ethylamine hydrochloride, obtained in stage B of Example 11, in 5 cm3 of pyridine. The reaction medium is stirred for 1 hour at a temperature of 80° C. and then poured into ice-cold water. The mixture is acidified with 1N hydrochloric acid solution. The precipitate formed is drained, washed with water, dried and then recrystallized in a toluene/cyclohexane mixture.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05420158uspto-grants-1995_05