| Identification | Back Directory | [Name]
4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER | [CAS]
821791-58-6 | [Synonyms]
ethyl 4-chloro-1-methyl-6-oxopyridine-3-carboxylate ethyl 4-chloro-1,6-dihydro-1-Methyl-6-oxopyridine-3-carboxylate ETHYL 4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDROPYRIDINE-3-CARBOXYLATE 4-CHLORO-1-METHYL-6-OXO-1,6-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID ETHYL ESTER 3-Pyridinecarboxylicacid, 4-chloro-1,6-dihydro-1-Methyl-6-oxo-, ethyl ester | [Molecular Formula]
C9H10ClNO3 | [MDL Number]
MFCD08234670 | [MOL File]
821791-58-6.mol | [Molecular Weight]
215.63 |
| Chemical Properties | Back Directory | [Boiling point ]
302.4±42.0 °C(Predicted) | [density ]
1.31±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
-3.05±0.62(Predicted) | [Appearance]
Yellow to brown Solid |
| Hazard Information | Back Directory | [Synthesis]
(Step 2) To ethyl 4-hydroxy-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate (9.2 g, 47 mmol) obtained in Step 1 was added phosphorous trichloride (26.1 mL, 280 mmol) and triethylamine (6.5 mL, 47 mmol). The reaction mixture was stirred at 50 °C for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and the solvent was removed by evaporation under reduced pressure. Saturated aqueous sodium bicarbonate (100 mL) was added to the residue, which was subsequently extracted with ethyl acetate (3 × 50 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford ethyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate (6.0 g, 60% yield). The product was confirmed by electrospray ionization mass spectrometry (ESIMS), m/z: 216 (M + H)+. | [References]
[1] Patent: EP2930170, 2015, A1. Location in patent: Paragraph 0253 [2] Journal of Medicinal Chemistry, 2006, vol. 49, # 2, p. 441 - 444 [3] Patent: US2005/256123, 2005, A1 |
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