Reaktion #972835

ord-4a332d112e6d42479324f6c5c6123f12

Reaktionsgleichung

[C-]#N.[Na+]
sodium cyanide
CCCCn1ccnc1
1-butyl-1H-imidazole
[Na+].[Na+].[O-]Cl.[OH-]
sodium hydroxide sodium hypochlorite
CNC(=O)c1cc(Br)cc(C)c1N
2-amino-5-bromo-N,3-dimethylbenzamide
Cc1cc(C)cc(C)c1
mesitylene
CNC(=O)c1cc(C#N)cc(C)c1N
title compound
CNC(=O)c1cc(C#N)cc(C)c1N
2-amino-5-cyano-N,3-dimethylbenzamide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 500-mL four-necked flask equipped with a mechanical stirrer
  2. 2
    workup.ADDITIONthermocouple, condenser, side-arm addition funnel
  3. 3
    Temperaturwhile maintaining an atmosphere of nitrogen through a gas inlet line
  4. 4
    TemperaturThe reaction mixture was heated
  5. 5
    Temperaturat reflux (about 166-170° C.) for 7 h
  6. 6
    TemperaturAfter cooling overnight
  7. 7
    workup.STIRRINGstirring
  8. 8
    FiltrationThe mixture was filtered
  9. 9
    Sonstigethe solid collected
  10. 10
    Waschenwas washed with water (3×50 mL), mesitylene (50 g)
  11. 11
    Sonstigedried to a constant weight in a vacuum-oven at 55° C.

Vorschrift

A 500-mL four-necked flask equipped with a mechanical stirrer, thermocouple, condenser, side-arm addition funnel and sodium hydroxide/sodium hypochlorite scrubber was charged with 2-amino-5-bromo-N,3-dimethylbenzamide (prepared by the method of Reference Example 1) (24.6 g, 0.10 mol, 99% purity) and mesitylene (100 g) while maintaining an atmosphere of nitrogen through a gas inlet line connected to the condenser. The reaction mixture was stirred at room temperature and sodium cyanide (ground to a powder just prior to use) (7.7 g, 0.15 mol, assuming 95% purity), copper(I) iodide (2.9 g, 0.015 mol, 98% purity) and 1-butyl-1H-imidazole (10.8 g, 0.085 mol, 98% purity) were added, after which time the nitrogen inlet line was attached directly to the reaction flask. The reaction mixture was heated at reflux (about 166-170° C.) for 7 h, while venting through the scrubber. After cooling overnight, water (100 mL) was added to the reaction mixture and stirring was continued for 1 h. The mixture was filtered, and the solid collected was washed with water (3×50 mL), mesitylene (50 g) and dried to a constant weight in a vacuum-oven at 55° C. to give the title compound as a light yellow solid (16.9 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08242279B2uspto-grants-2012_08