| Identification | Back Directory | [Name]
5-CARBOXY-N-PHENYL-2-1H-PYRIDONE | [CAS]
77837-08-2 | [Synonyms]
5-Carboxy Pirfenidone 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylic Acid 1,6-Dihydro-6-oxo-1-phenyl-3-pyridinecarboxylic Acid | [Molecular Formula]
C12H9NO3 | [MDL Number]
MFCD07369218 | [MOL File]
77837-08-2.mol | [Molecular Weight]
215.2 |
| Chemical Properties | Back Directory | [Appearance]
Off-White Fluffy Solid | [Melting point ]
282-284°C | [storage temp. ]
-20°C Freezer | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
Off-White to Light Yellow |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Fluffy Solid | [Uses]
A metabolite of Pirfenidone, a new drug to treat patients with kidney disease who have diabetes | [Synthesis]
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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