Methyl 5-carboxy-N-phenyl-2-1H-pyridone

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Methyl 5-carboxy-N-phenyl-2-1H-pyridone Basic information
Product Name:Methyl 5-carboxy-N-phenyl-2-1H-pyridone
Synonyms:3-Pyridinecarboxylicacid, 1,6-dihydro-6-oxo-1-phenyl-, methyl ester;1,6-Dihydro-6-oxo-1-phenyl-nicotinic Acid Methyl Ester;Methyl 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate;6-Oxo-1-phenyl-1,6-dihydro-pyridine-3-carboxylic acid methyl ester;irfenidone 5-Carboxylate Methyl Ester;Methyl 1,6-dihydro-6-oxo-1-phenylpyridine-3-carboxylate;Methyl 1,6-dihydro-6-oxo-1-phenyl-3-pyridinecarboxylate
CAS:77837-09-3
MF:C13H11NO3
MW:229.23
EINECS:
Product Categories:Aromatics Compounds;Aromatics;Metabolites;Metabolites & Impurities
Mol File:77837-09-3.mol
Methyl 5-carboxy-N-phenyl-2-1H-pyridone Structure
Methyl 5-carboxy-N-phenyl-2-1H-pyridone Chemical Properties
Melting point 160-162 °C
Boiling point 370.0±42.0 °C(Predicted)
density 1.270±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka-1.40±0.63(Predicted)
Safety Information
MSDS Information
Methyl 5-carboxy-N-phenyl-2-1H-pyridone Usage And Synthesis
Chemical PropertiesWhite Solid
UsesA metabolite of Pirfenidone, a new drug to treat patients with kidney disease who have diabetes.
Synthesis
METHYL 6-OXO-1,6-DIHYDRO-3-PYRIDINECARBOXYLATE

66171-50-4

Phenylboronic acid

98-80-6

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

77837-09-3

Methyl 6-hydroxynicotinate (6.0 g, 39.22 mmol) and phenylboronic acid (5.74 g, 47.06 mmol) were added copper(II) acetate monohydrate (11.76 g, 58.82 mmol), pyridine (6.32 mL, 78.43 mmol), and molecular sieves (4, 6.0 g) in dichloromethane (100 mL). The reaction mixture was stirred at ambient temperature for 12 h and then filtered. After standard post-extraction treatment the crude product was obtained and purified by silica gel column chromatography (100-200 mesh, eluent chloroform solution containing 1-2% methanol) to afford methyl 6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carboxylate as a brown solid (5.0 g, 56% yield). The product has a melting point of 100-105°C. 1H NMR (400 MHz, CDCl3) δ 3.86 (s, 3H), 6.63 (d, J = 9.5 Hz, 1H), 7.36-7.55 (m, 5H), 7.91 (dd, J = 2.5, 9.9 Hz, 1H), 8.23 (d, J = 2.5 Hz, 1H); IR (KBr ) ν 3058, 2924, 2854, 1721, 1675, 1540, 1446, 1313, 1271, 1103 cm-1; MS 230 (M + 1).

References[1] Patent: US2008/319026, 2008, A1. Location in patent: Page/Page column 22
[2] Patent: WO2012/122165, 2012, A2. Location in patent: Page/Page column 63
Methyl 5-carboxy-N-phenyl-2-1H-pyridone Preparation Products And Raw materials
Raw materialsMethyl 6-oxo-1,6-dihydro-3-pyridinecarboxylate-->Phenylboronic acid-->Dichloromethane-->Molecular sieve 3A-->Copper(II) acetate-->Pyridine
Preparation Products5-Carboxy-N-phenyl-2-1H-pyridone
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