Реакция #302869

ord-44311b2c45b94b29b982197b92097dfa

Уравнение реакции

CO
Methanol
O=S(Cl)Cl
thionyl chloride
Nc1ncccc1C(=O)O
2-aminonicotinic acid
COC(=O)c1cccnc1N
2-aminonicotinic acid methyl ester
Выход 55.0%

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was heated
  2. 2
    Температураto reflux
  3. 3
    Температураthe mixture was refluxed for 19 hours
  4. 4
    ДругоеThe solvent was removed under reduced pressure
  5. 5
    workup.ADDITIONThe residue was carefully treated with a satured NaHCO3 solution
  6. 6
    Экстракцияextracted with ethyl acetate
  7. 7
    СушкаThe organic fraction was dried over magnesium sulfate
  8. 8
    Другоеthe solvent was evaporated under reduced pressure

Методика

42.4 g (356.4 mmol, 26 ml) thionyl chloride was added dropwise to a suspension of 15.0 g (108.6 mmol) 2-aminonicotinic acid in 150 ml abs. Methanol, while cooling. The mixture was heated to reflux and the mixture was refluxed for 19 hours. The evolving SO2 was scrubbed. The solvent was removed under reduced pressure after cooling down to room temperature. The residue was carefully treated with a satured NaHCO3 solution and extracted with ethyl acetate. The organic fraction was dried over magnesium sulfate and the solvent was evaporated under reduced pressure. 9.13 g (55%) of 2-aminonicotinic acid methyl ester was isolated as a pale yellow solid (m.p. 83° C.).

Источник

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