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| | Methyl 3-chloroisonicotinate Basic information |
| Product Name: | Methyl 3-chloroisonicotinate | | Synonyms: | 3-Chloropyridine-4-carboxylic acid methyl ester;Methyl 3-chloropyridine-4-carboxylate;3-Chloro-4-pyridinecarboxylic acid methyl ester;Methyl 3-chloronicotinate;Methyl 3-chloroisonicotinate;4-Pyridinecarboxylic acid, 3-chloro-, methyl ester | | CAS: | 98273-79-1 | | MF: | C7H6ClNO2 | | MW: | 171.58 | | EINECS: | | | Product Categories: | pharmacetical | | Mol File: | 98273-79-1.mol |  |
| | Methyl 3-chloroisonicotinate Chemical Properties |
| Boiling point | 70-75℃ (0.1 Torr) | | density | 1.294±0.06 g/cm3(Predicted) | | refractive index | 1.53425 (589.3 nm 20℃) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | pka | 0.83±0.18(Predicted) | | Appearance | Colorless to light yellow Liquid |
| | Methyl 3-chloroisonicotinate Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of methyl 3-chloroisonicotinate from 3-chloropyridine-4-carboxylic acid and iodomethane was as follows: potassium carbonate (36.3 g, 263 mmol) was added to 3-chloropyridine-4-carboxylic acid (10.35 g, 65.7 mmol) dissolved in DMSO (50 mL). After 30 min of reaction, iodomethane (8.22 mL, 131 mmol) was slowly added. The reaction mixture was stirred continuously at room temperature for 2 hours. Upon completion of the reaction, the reaction was quenched with saturated ammonium chloride solution (300 mL) and deionized water (200 mL), followed by extraction with ethyl acetate (3 x 200 mL). The organic phases were combined, washed with brine (2 × 50 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to remove the solvent. Purification by silica gel column chromatography with the eluent being a hexane solution of 10-30% ethyl acetate resulted in methyl 3-chloroisonicotinate as a colorless liquid (6.275 g, 56% yield). MS (electrospray positive ion mode) m/z: 172 ([M+H]+); LC retention time: 2.45 min (analytical conditions). | | References | [1] Patent: WO2009/100171, 2009, A1. Location in patent: Page/Page column 70
[2] Synthetic Communications, 1997, vol. 27, # 6, p. 1075 - 1086 |
| | Methyl 3-chloroisonicotinate Preparation Products And Raw materials |
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