Reaction #44705

ord-e71ce06648664f55b7b56df2f5f3a739

Reaction equation

O=P(Cl)(Cl)Cl
phosphoryl chloride
N#Cc1cccc(-c2cc(=O)[nH]c(N)n2)c1
3-(2-amino-6-oxo-1,6-dihydropyrimidin-4-yl)benzonitrile
CCN(CC)c1ccccc1
N,N-diethylaniline
N#Cc1cccc(-c2cc(Cl)nc(N)n2)c1
title compound
N#Cc1cccc(-c2cc(Cl)nc(N)n2)c1
3-(2-Amino-6-chloropyrimidin-4-yl)benzonitrile

Conditions

Temperature
115°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.WAITover a period of a further hour
  2. 2
    TemperatureThe mixture is then heated at RF for one hour
  3. 3
    Temperatureto cool to RT
  4. 4
    ExtractionThe mixture is extracted twice with ethyl acetate
  5. 5
    Otherthe solvent is removed under reduced pressure
  6. 6
    TemperatureWith ice-cooling
  7. 7
    workup.ADDITIONthe solution is neutralized by addition of conc. sodium hydroxide solution
  8. 8
    workup.ADDITIONSaturated sodium carbonate solution is added
  9. 9
    FiltrationThe precipitate is filtered off with suction
  10. 10
    Washwashed with water

Procedure

2.00 g (9.42 mmol) of 3-(2-amino-6-oxo-1,6-dihydropyrimidin-4-yl)benzonitrile (from example LV) are suspended in 10 ml of phosphoryl chloride. Over a period of one hour, 180 mg (1.23 mmol) of N,N-diethylaniline are added dropwise, and over a period of a further hour, the mixture is heated to 115° C. The mixture is then heated at RF for one hour. The mixture is allowed to cool to RT and poured into ice water. The mixture is extracted twice with ethyl acetate and the solvent is removed under reduced pressure. The residue is suspended in water. With ice-cooling, the solution is neutralized by addition of conc. sodium hydroxide solution. Saturated sodium carbonate solution is added, and the mixture is stirred at RT overnight. The precipitate is filtered off with suction and washed with water. This gives the title compound.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737153B2uspto-grants-2010_06