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3-Amino-2-pyridinecarboxylic acid

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CAS:1462-86-8
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3-Amino-2-pyridinecarboxylic acid manufacturers

3-Amino-2-pyridinecarboxylic acid Basic information
Product Name:3-Amino-2-pyridinecarboxylic acid
Synonyms:IFLAB-BB F2113-0045;H-3APC2-OH;RARECHEM AQ NN 0176;3-amino-2-pyridinecarboxylicaci;3-AMINO-2-PYRIDINECARBOXYLIC ACID;3-AMINO-PYRIDINE-2-CARBOXYLIC ACID;3-AMINOPICOLINIC ACID;AKOS 92172
CAS:1462-86-8
MF:C6H6N2O2
MW:138.12
EINECS:215-971-8
Product Categories:Heterocycle-Pyridine series;AMINOACID;Amines;Heterocycles;Pyridine;pharmacetical;Pyridine series;Carboxylic Acids;Pyridines;Organic acids;Aromatics Compounds;Aromatics;Carboxylic Acids
Mol File:1462-86-8.mol
3-Amino-2-pyridinecarboxylic acid Structure
3-Amino-2-pyridinecarboxylic acid Chemical Properties
Melting point 218-220
Boiling point 386.6±27.0 °C(Predicted)
density 1.417±0.06 g/cm3(Predicted)
RTECS US5175000
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility Soluble in acetone, ethanol and methanol.
form Solid
pka1.32±0.50(Predicted)
color Yellow to pale brown
InChIInChI=1S/C6H6N2O2/c7-4-2-1-3-8-5(4)6(9)10/h1-3H,7H2,(H,9,10)
InChIKeyBOOMHTFCWOJWFO-UHFFFAOYSA-N
SMILESC1(C(O)=O)=NC=CC=C1N
CAS DataBase Reference1462-86-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37-60
HazardClass IRRITANT
HS Code 29333990
MSDS Information
3-Amino-2-pyridinecarboxylic acid Usage And Synthesis
Chemical PropertiesGreen/Brown Crystals
Uses3-Amino-2-pyridinecarboxylic acid is a useful synthetic intermediate.
UsesEmployed as an important intermediate for syntheses material and pharmaceutical.
Application3-Aminopicolinic Acid is used in the preparation of piperidinyl-methyl-purinamines as NSD2 inhibitors and anti-cancer agents.
Synthesis
3-NITRO-PYRIDINE-2-CARBOXYLIC ACID

59290-85-6

3-Amino-2-pyridinecarboxylic acid

1462-86-8

(2) Preparation of 3-aminopyridine-2-carboxylic acid: 3-nitropyridine-2-carboxylic acid (2.72 g, 16.2 mmol) and sodium bicarbonate (1.34 g, 16.2 mmol) were dissolved in distilled water (20 mL). The atmosphere in the system was replaced with nitrogen to exclude oxygen. After adding 10% palladium carbon catalyst (1.72 g), the atmosphere in the system was replaced with hydrogen and the reaction was stirred at room temperature for 50 hours. After completion of the reaction, the pH of the reaction solution was adjusted to weakly acidic by adding 1N aqueous hydrochloric acid. The solvent was removed by distillation under reduced pressure and a small amount of ethanol and ethyl acetate was added to the residue and the resulting precipitate was collected by filtration. The filtrate was concentrated to afford the target product 3-aminopyridine-2-carboxylic acid (1.50 g, 67% yield) as a light yellow solid.

References[1] Patent: US2005/182045, 2005, A1. Location in patent: Page/Page column 74
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