Реакция #302867

ord-b2fff7c590ea4b8b851c57434f503c61

Уравнение реакции

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
Выход 97.0%

Растворители

Условия реакции

Температура
40°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling down to room temperature
  2. 2
    Другоеthe formed precipitate is removed by filtration
  3. 3
    Концентрированиеthe filtrate is concentrated to dryness

Методика

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.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08192918B2uspto-grants-2012_06