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| | Methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate Basic information |
| Product Name: | Methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate | | Synonyms: | METHYL 2-OXO-1,2-DIHYDRO-3-PYRIDINECARBOXYLATE;SPECS AE-508/36398048;3-Pyridinecarboxylic acid, 1,2-dihydro-2-oxo-, methyl ester;Methyl 1,2-dihydro-2-oxopyridine-3-carboxylate;2-Hydroxy-nicotinic acid methyl ester;Methyl 6-hydroxypyridin-3-carboxylate;1,2-Dihydro-3-(methoxycarbonyl)-2-oxopyridine;Methyl 2-oxo-l,2-dihydropyridine-3-carboxylate | | CAS: | 10128-91-3 | | MF: | C7H7NO3 | | MW: | 153.14 | | EINECS: | | | Product Categories: | Esters;Pyridines | | Mol File: | 10128-91-3.mol |  |
| | Methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate Chemical Properties |
| Melting point | 115-118°C | | Boiling point | 367.6±42.0 °C(Predicted) | | density | 1.263±0.06 g/cm3(Predicted) | | storage temp. | Inert atmosphere,Room Temperature | | pka | 10.07±0.10(Predicted) | | form | Solid | | color | Cream |
| HazardClass | IRRITANT | | HS Code | 2933399990 |
| | Methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate Usage And Synthesis |
| Uses |
Methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate is a crucial compound that could be used as a pharmaceutical intermediate in pharmaceutical synthesis and scientific research.
| | Synthesis | Sulfuric acid (15 mL) and toluene (100 mL) were added to a concentrated solution of 2-hydroxynicotinic acid (50 g) in methanol (500 mL). The reaction mixture was stirred at room temperature for 28 hours before a Dean-Stark reflux device was installed and the reaction solution was neutralized with aqueous potassium carbonate, followed by evaporation of the solvent. Saturated aqueous ammonium chloride and chloroform were added to the residue, the organic layer was separated and the aqueous layer was extracted with chloroform. The organic layers were combined, dried with anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to afford methyl 2-hydroxynicotinate (46 g, 84% yield) as a white solid.1H NMR (300 MHz, CDCl3) δ: 3.92 (s, 3H), 6.45 (dd, J=7.3,6.4 Hz, 1H), 7.78 (dd, J=6.4,2.4 Hz, 1H). 8.29 (dd, J=7.3,2.4Hz, 1H). | | References | [1] Patent: EP1477186, 2004, A1. Location in patent: Page/Page column 41
[2] Patent: EP1357111, 2003, A1. Location in patent: Page/Page column 59-60
[3] European Journal of Medicinal Chemistry, 2012, vol. 52, p. 284 - 294
[4] Patent: US2013/317059, 2013, A1. Location in patent: Paragraph 0404
[5] Patent: JP2016/124812, 2016, A. Location in patent: Paragraph 0331 |
| | Methyl 2-oxo-1,2-dihydro-3-pyridinecarboxylate Preparation Products And Raw materials |
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