Reaktion #302868

ord-0699d80eb7304ff3a7e18c94bde50429

Reaktionsgleichung

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
Ausbeute 67.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
55°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto cool down to room temperature
  2. 2
    Sonstige3-methyl-1H-pyrido[2,3-d]pyrimidine-2,4-dione crystallized from the medium
  3. 3
    Sonstigewas isolated by filtration
  4. 4
    Waschenwashed with water, methanol and tert.-butyl methyl ether

Vorschrift

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.).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08192918B2uspto-grants-2012_06