Réaction #582539

ord-a9227a6d4dc548e19e26e82e61c7cba6

Équation de réaction

NC=O
formamide
Nc1c(Br)cc(Cl)cc1C(=O)O
2-amino-3-bromo-5-chlorobenzoic acid
O=c1[nH]cnc2c(Br)cc(Cl)cc12
8-Bromo-6-chloro-4(3H) quinazolinone

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureat reflux overnight
  2. 2
    TempératureThe mixture was cooled
  3. 3
    Autrequenched with water
  4. 4
    AutreThe solid that formed
  5. 5
    Lavagewas washed with acetonitrile, 6.7 g crude (65%)

Mode opératoire

8-Bromo-6-chloro-4(3H) quinazolinone was prepared from 2-amino-3-bromo-5-chlorobenzoic acid (10 g, 40 mmol). The acid was heated in excess formamide (50 mL) at reflux overnight. The mixture was cooled and quenched with water. The solid that formed was washed with acetonitrile, 6.7 g crude (65%); MS: 260.8 (M+H)+

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06939870B2uspto-grants-2005_09