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3-METHYL-PYRIDINE-4-CARBOXAMIDE

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3-METHYL-PYRIDINE-4-CARBOXAMIDE Basic information

Product Name:
3-METHYL-PYRIDINE-4-CARBOXAMIDE
Synonyms:
  • 3-METHYL-PYRIDINE-4-CARBOXAMIDE
  • 2-carbaMoyl-3-Methylpyridine-4-carboxylic acid
  • 4-Pyridinecarboxamide,3-methyl-(9CI)
  • 3-Methylisonicotinamide
  • 4-Pyridinecarboxamide, 3-methyl-
CAS:
251101-36-7
MF:
C7H8N2O
MW:
136.15
Product Categories:
  • Pyridines
  • PYRIDINE
  • AMIDE
Mol File:
251101-36-7.mol
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3-METHYL-PYRIDINE-4-CARBOXAMIDE Chemical Properties

Boiling point:
290.8±28.0 °C(Predicted)
Density 
1.157±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
14.98±0.50(Predicted)
InChI
InChI=1S/C7H8N2O/c1-5-4-9-3-2-6(5)7(8)10/h2-4H,1H3,(H2,8,10)
InChIKey
QMDMUIQZTHZWGH-UHFFFAOYSA-N
SMILES
C1=NC=CC(C(N)=O)=C1C
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Safety Information

HS Code 
2933399990
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3-METHYL-PYRIDINE-4-CARBOXAMIDE Usage And Synthesis

Synthesis

4021-12-9

251101-36-7

General procedure for the synthesis of 3-methylpyridine-4-carboxamide from 3-methyl-4-pyridinecarboxylic acid: 3-methyl-4-pyridinecarboxylic acid (0.5 g, 3.6 mmol) was dissolved in thionyl chloride (3 mL) and heated to reflux for 3 hours. Upon completion of the reaction, the excess thionyl chloride was removed by evaporation under reduced pressure. The resulting chloride solid was added to ammonium hydroxide solution (30 mL, 25% aqueous solution) in batches under ice bath conditions. Subsequently, the reaction mixture was slowly warmed to room temperature and stirred for 10 minutes. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by silica gel fast column chromatography (eluent: methanol/dichloromethane, 40:1) to give a white solid product in 63% yield. The product was characterized by 1H NMR (400 MHz, CD3OD): δ 8.50-8.48 (m, 1H), 8.46-8.44 (m, 1H), 7.42 (d, J = 5.0 Hz, 1H), 2.45 (s, 3H).

References

[1] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 12, p. 3559 - 3572
[2] Journal of Medicinal Chemistry, 2012, vol. 55, # 4, p. 1682 - 1697
[3] Patent: US2014/18360, 2014, A1
[4] Chemistry - A European Journal, 2016, vol. 22, # 24, p. 8301 - 8308

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