Réaction #302868

ord-0699d80eb7304ff3a7e18c94bde50429

Équation de réaction

CNC(=O)c1cccnc1N
2-aminonicotinic acid methyl amide
O=C(Oc1ccccc1)Oc1ccccc1
diphenyl carbonate
Cn1c(=O)[nH]c2ncccc2c1=O
3-methyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione
Rendement 67.0%

Solvants

Conditions de réaction

Température
55°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureto cool down to room temperature
  2. 2
    Autre3-methyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione crystallized from the medium
  3. 3
    Autrewas isolated by filtration
  4. 4
    Lavagewashed with water, methanol and tert.-butyl methyl ether

Mode opératoire

10.0 g (66 mmol) of 2-aminonicotinic acid methyl amide, 21.4 g (100 mmol) diphenyl carbonate and 8.5 g (66 mmol) 4-dimethylaminopyridine were melted at 140 to 150° C. The reaction was allowed to continue for 20 minutes at that temperature. The mixture is allowed to cool down to 50 to 60° C. and 300 ml methanol was added while stirring. The mixture is allowed to cool down to room temperature. 3-methyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione crystallized from the medium, was isolated by filtration and washed with water, methanol and tert.-butyl methyl ether. 7.80 g (67%) of 3-methyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione was isolated (m.p. 272-4° C.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08192918B2uspto-grants-2012_06