Ethanol → Ethyl 6-Aminopyridine-2-carboxylate

HRID 2359447Notes

Reaction equation

HRID 2359447 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]([OH:10])=[O:9])[N:3]=1.O=S(Cl)Cl.[CH2:15](O)[CH3:16]>>[NH2:1][C:2]1[N:3]=[C:4]([C:8]([O:10][CH2:15][CH3:16])=[O:9])[CH:5]=[CH:6][CH:7]=1

Participants

4

Procedure

To a solution of 2-amino-6-pyridinecarboxylic acid (6.0 g, 43.5 mmol) in ethanol (150 mL) was added SOCl2 (12.0 g, 101 mmol) at 0° C. The resulting reaction mixture was stirred under reflux for 12 h. Upon cooling to room temperature, the reaction mixture was concentrated under reduced pressure. Enough saturated aqueous Na2CO3 solution was added to adjust the pH=9. The mixture was concentrated under reduced pressure and dichloromethane (150 mL) was added to the resulting residue. The mixture was stirred vigorously at room temperature for 30 min and then filtered. The filtrate was concentrated under reduced pressure to afford ethyl 6-aminopicolinate (5.5 g, 76%).

Workup

  1. customThe resulting reaction mixture
  2. temperatureunder reflux for 12 h
  3. concentrationthe reaction mixture was concentrated under reduced pressure
  4. additionEnough saturated aqueous Na2CO3 solution was added
  5. concentrationThe mixture was concentrated under reduced pressure and dichloromethane (150 mL)
  6. additionwas added to the resulting residue
  7. stirringThe mixture was stirred vigorously at room temperature for 30 min
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-12a4cfdc2e524883b468513c2e5c9ea5
Source dataset
uspto-grants-2014_04
Patent number
US08685970B2

Reaction notes

Loading…