Reaktion #302867

ord-b2fff7c590ea4b8b851c57434f503c61

Reaktionsgleichung

NC(=O)[O-]
carbamate
O=C1CC(=O)C2=C(C=NOC2)N1
1H-Pyrido[2,3-d]oxazin-2,4-dione
CN
methyl amine
O=C=O
CO2
CNC(=O)c1cccnc1N
2-aminonicotinic acid methyl amide
Ausbeute 97.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
40°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter cooling down to room temperature
  2. 2
    Sonstigethe formed precipitate is removed by filtration
  3. 3
    Einengenthe filtrate is concentrated to dryness

Vorschrift

14.96 g (0.09 mol) of 1H-Pyrido[2,3-d]oxazin-2,4-dione was suspended in 138 ml dioxane. The mixture is heated to 40° C. and 17 ml of a 33% solution of methyl amine in ethanol is added dropwise directly into the reaction mixture, to avoid carbamate formation with the evolving CO2. The reaction is allowed to continue for 90 minutes. After cooling down to room temperature, the formed precipitate is removed by filtration and the filtrate is concentrated to dryness. 13.2 g (97%) of 2-aminonicotinic acid methyl amide was isolated (m.p. 140-2° C.).

Quelle

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