Malonic Acid → 3-Amino-3-(pyridin-3-yl)propanoic acid

反応式

[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1C=O.C([O-])(=O)C.[NH4+:13].[C:14](O)(=O)[CH2:15][C:16]([OH:18])=[O:17]>C(O)(C)C>[NH2:13][CH:14]([C:5]1[CH:6]=[N:1][CH:2]=[CH:3][CH:4]=1)[CH2:15][C:16]([OH:18])=[O:17]

参加物

実験手順

Scheme I describes a synthesis of a pyridyl β-amino acid which can be used to synthesize compounds of the present invention wherein R1 is pyridyl. The reaction can be modified using conventional methodology to prepare other aroma substituted or heterocyclic substituted β-amino acids by substitution of the pyridyl carboxaldehyde with any other appropriate aldehyde. Briefly, in Scheme I to pyridine-carboxaldehyde in isopropanol is added ammonium acetate followed by malonic acid. The reaction mixture is stirred at reflux, the resulting precipitate filtered and washed with hot isopropanol and dried to yield 3-amino-3-(3-pyridyl)propionic acid. The ethyl ester is synthesized by heating this acid in excess ethanol in the presence of excess HCl gas.