Basic information Safety Supplier Related

5-CARBOXY-N-PHENYL-2-1H-PYRIDONE

Basic information Safety Supplier Related

5-CARBOXY-N-PHENYL-2-1H-PYRIDONE Basic information

Product Name:
5-CARBOXY-N-PHENYL-2-1H-PYRIDONE
Synonyms:
  • 6-oxo-1-phenyl-1,6-dihydro-3-pyridinecarboxylic acid
  • 6-oxo-1-phenylpyridine-3-carboxylic acid
  • 1,6-Dihydro-6-oxo-1-phenyl-3-pyridinecarboxylic Acid
  • 5-Carboxy Pirfenidone
  • 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylic Acid
  • 5-carboxy-N-phenyl-2-pyridone
  • 3-Pyridinecarboxylicacid, 1,6-dihydro-6-oxo-1-phenyl-
CAS:
77837-08-2
MF:
C12H9NO3
MW:
215.2
Product Categories:
  • Aromatics
  • Metabolites
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Metabolites & Impurities
  • Pharmaceuticals
Mol File:
77837-08-2.mol
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5-CARBOXY-N-PHENYL-2-1H-PYRIDONE Chemical Properties

Melting point:
282-284°C
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
Off-White to Light Yellow
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5-CARBOXY-N-PHENYL-2-1H-PYRIDONE Usage And Synthesis

Chemical Properties

Off-White Fluffy Solid

Uses

A metabolite of Pirfenidone, a new drug to treat patients with kidney disease who have diabetes.

Synthesis

77837-09-3

77837-08-2

General procedure for the synthesis of 6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carboxylic acid from methyl 6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carboxylate: at 0 °C, lithium hydroxide monohydrate (0.366 g, 8.73 mmol) was added to a mixed solution of tetrahydrofuran (9 mL) and water (6 mL) containing methyl 6-oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate (1.0 g, 4.37 mmol) in a mixed solution of tetrahydrofuran (9 mL) and water (6 mL) and the reaction was stirred for 1 hour. After completion of the reaction, the reaction mixture was diluted with water and washed with ethyl acetate. Subsequently, the pH of the aqueous layer was adjusted to 2 with 2N hydrochloric acid and the precipitate was collected by filtration to afford 6-oxo-1-phenyl-1,6-dihydropyridine-3-carboxylic acid as a brown solid (0.740 g, 79% yield). The melting point of the product was 256-263°C. The structure of the product was determined by 1H NMR (400 MHz, DMSO-d6) δ 6.53 (d, J = 9.4 Hz, 1H), 7.40-7.49 (m, 5H), 7.87 (dd, J = 2.5, 9.8 Hz, 1H), 8.23 (d, J = 2.5 Hz, 1H); IR (KBr) ν 3446, 1708, 1645, 1577, 1263, 1228 cm-1; MS 214 (M-1) for characterization.

References

[1] Archiv der Pharmazie, 2013, vol. 346, # 9, p. 654 - 666
[2] Patent: US2008/319026, 2008, A1. Location in patent: Page/Page column 22
[3] Patent: WO2012/122165, 2012, A2. Location in patent: Page/Page column 63-64
[4] Patent: US2013/317059, 2013, A1. Location in patent: Paragraph 0042-0043
[5] Journal of Medicinal Chemistry, 2013, vol. 56, # 12, p. 5079 - 5093

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