Ethyl Acrylate → Ethyl 3-(pyridin-2-ylamino)propanoate

HRID 1527145Notes

Reaction equation

HRID 1527145 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[C:8]([O:12][CH2:13][CH3:14])(=[O:11])[CH:9]=[CH2:10]>C(O)(=O)C>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:1][CH2:10][CH2:9][C:8]([O:12][CH2:13][CH3:14])=[O:11]

Participants

4

Conditions

Temperature
88 °C

Procedure

200 g (2.12 mol) of 2-aminopyridine and 346 mL (3.19 mol) of ethyl acrylate were dissolved in 53 mL of acetic acid. The mixture was heated to 88° C. and stirred overnight at this temperature. Solvent was removed under vacuum, and the title compound was purified by column chromatography, eluting with ethyl acetate, to obtain 360 g of ethyl 3-(2-pyridylamino)propionate as a white solid. Yield: 86.7%.

Workup

  1. customSolvent was removed under vacuum
  2. customthe title compound was purified by column chromatography
  3. washeluting with ethyl acetate

Sources & evidence

ORD record
ord-2fb8517b37cf413eb1cfe529ce5a824c
Source dataset
uspto-grants-2015_07
Patent number
US09086390B2

Reaction notes

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