Reaktion #578153

ord-ebbb23c7f0d44b34bf244cb2203da18f

Reaktionsgleichung

O
water
CC(=O)O
acetic acid
Cc1cc(Cl)cc2c(=O)oc(=O)[nH]c12
6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione
CN
methylamine
CNC(=O)c1cc(Cl)cc(C)c1N
title compound
Ausbeute 87.0%
CNC(=O)c1cc(Cl)cc(C)c1N
2-amino-5-chloro-N,3-dimethylbenzamide
Ausbeute 87.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred for 30 minutes at this temperature
  2. 2
    FiltrationThe suspension was then filtered
  3. 3
    Waschenthe solids were washed with water (3×200 mL)
  4. 4
    Sonstigedried under nitrogen

Vorschrift

To a suspension of 6-chloro-8-methyl-2H-3,1-benzoxazine-2,4(1H)-dione (211.6 g, 1000 mmol) in acetonitrile (700 mL) was added acetic acid (7.3 g, 122 mmol). Then 40% aqueous methylamine (104 mL) was added dropwise over 30 minutes at 25-30° C. Stirring was continued for 2 h, and then water (700 mL) was added slowly. The resulting suspension was cooled to 5° C., and stirred for 30 minutes at this temperature. The suspension was then filtered, and the solids were washed with water (3×200 mL) and dried under nitrogen to afford the title compound as off-white needles, 172.8 g (87.0% yield), m.p. 141-143° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07528260B2uspto-grants-2009_05