Reaktion #80912

ord-2fd8e3f976db4526a37d349461763896

Reaktionsgleichung

Cc1c([N+](=O)[O-])ccc(Cl)c1C#N
2-chloro-6-methyl-5-nitrobenzonitrile
N=C(N)N.O=C(O)O
guanidine carbonate
Cc1c([N+](=O)[O-])ccc2nc(N)nc(N)c12
2,4-diamino-5-methyl-6-nitroquinazoline
Ausbeute 82.7%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux during a 3.5 hour period
  2. 2
    EinengenAfter this time, the reaction mixture was concentrated under reduced pressure to a residue
  3. 3
    Filtrationthe resultant solid was collected by filtration
  4. 4
    WaschenThe solid was washed with 50 mL of water
  5. 5
    Sonstigedried under reduced pressure

Vorschrift

Under a nitrogen atmosphere, a stirred solution 29.5 grams (0.150 mole) of 2-chloro-6-methyl-5-nitrobenzonitrile and 54.0 grams (0.300 mole) of guanidine carbonate in 1500 mL of 2-ethoxyethanol was heated at reflux during a 3.5 hour period. After this time, the reaction mixture was concentrated under reduced pressure to a residue. The residue was stirred with 300 mL of water, and the resultant solid was collected by filtration. The solid was washed with 50 mL of water and dried under reduced pressure, yielding 27.2 grams of 2,4-diamino-5-methyl-6-nitroquinazoline. The NMR spectrum was consistent with the proposed structure. The reaction was repeated again.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05616718uspto-grants-1997_04