methyl quinoline-3-carboxylate
methyl quinoline-3-carboxylate Basic information
- Product Name:
- methyl quinoline-3-carboxylate
- Synonyms:
-
- Methyl 3-quinolinecarboxylate
- methyl quinoline-3-carboxylate
- 3-Quinolinecarboxylic acid, methyl ester
- Quinoline-3-carboxylic acid methyl ester
- Methyl-Quinolone-3-Carboxylate
- CAS:
- 53951-84-1
- MF:
- C11H9NO2
- MW:
- 187.19
- Product Categories:
-
- API intermediates
- Esters
- Quinolines, Isoquinolines & Quinoxalines
- Mol File:
- 53951-84-1.mol
methyl quinoline-3-carboxylate Chemical Properties
- Melting point:
- 73-74 °C
- Boiling point:
- 294.5±13.0 °C(Predicted)
- Density
- 1.210±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 3.11±0.11(Predicted)
- Appearance
- Off-white to light yellow Solid
methyl quinoline-3-carboxylate Usage And Synthesis
Synthesis Reference(s)
Journal of Medicinal Chemistry, 25, p. 1081, 1982 DOI: 10.1021/jm00351a015
Synthesis
67-56-1
6480-68-8
53951-84-1
General procedure for the synthesis of methyl 3-quinolinecarboxylate from methanol and quinoline-3-carboxylic acid: quinoline-3-carboxylic acid (3 g, 17.32 mmol) was dissolved in methanol (30 mL) and cooled at 0°C in an ice bath. Subsequently, thionyl chloride (1.264 mL, 17.32 mmol) was added slowly and dropwise, then the reaction mixture was heated to 80°C and kept overnight. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the methanol was evaporated under reduced pressure and the resulting residue was alkalized with saturated sodium bicarbonate solution to pH 7 to 8, precipitating a white solid. After filtration and drying, methyl 3-quinolinecarboxylate (3.2 g, 99% yield) was obtained as a white solid; mass spectrometry (M/Z) showed a molecular ion peak of 187.3.
References
[1] Patent: WO2014/33604, 2014, A1. Location in patent: Page/Page column 48
[2] Organic and Biomolecular Chemistry, 2016, vol. 14, # 24, p. 5505 - 5510
[3] Tetrahedron Asymmetry, 2013, vol. 24, # 18, p. 1142 - 1147
[4] Patent: US2016/122303, 2016, A1. Location in patent: Paragraph 0078
[5] Tetrahedron Asymmetry, 2010, vol. 21, # 18, p. 2307 - 2313
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