ChemicalBook--->CAS DataBase List--->849807-09-6

849807-09-6

849807-09-6 Structure

849807-09-6 Structure
IdentificationBack Directory
[Name]

methyl 2-chloroquinoline-6-carboxylate
[CAS]

849807-09-6
[Synonyms]

methyl 2-chloroquinoline-6-carboxylate
6-Quinolinecarboxylic acid, 2-chloro-, methyl ester
[Molecular Formula]

C11H8ClNO2
[MDL Number]

MFCD17215626
[MOL File]

849807-09-6.mol
[Molecular Weight]

221.64
Chemical PropertiesBack Directory
[Melting point ]

134-136 °C(Solv: chloroform (67-66-3))
[Boiling point ]

343.7±22.0 °C(Predicted)
[density ]

1.330±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

-0.60±0.43(Predicted)
[Appearance]

Off-white to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 2-chloroquinoline-6-carboxylate (849807-09-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Quinolinecarboxylic acid, methyl ester, 1-oxide

358368-09-9

methyl 2-chloroquinoline-6-carboxylate

849807-09-6

To a dichloromethane solution of 2-chloroquinoline-6-carboxylic acid (4.0 g, 20 mmol) and N,N-dimethylformamide (8 ml) was slowly added sulfoxide chloride (8 ml) at 0°C and the reaction mixture was stirred for 5 hours at room temperature. After completion of the reaction, the mixture was concentrated to give a residue. The residue was dissolved in dichloromethane (50 ml) and washed with saturated sodium bicarbonate solution (20 ml) and stirred for 30 minutes. The organic layer was separated and concentrated to give the crude product. The crude product was purified by silica gel column chromatography to afford methyl 2-chloroquinoline-6-carboxylate (1.3 g, 30% yield) as a white solid.

[References]

[1] European Journal of Organic Chemistry, 2016, vol. 2016, # 8, p. 1606 - 1611
[2] Patent: US2014/128391, 2014, A1. Location in patent: Paragraph 0188; 0191; 0192; 0282; 0285; 0286
[3] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 12, p. 3573 - 3578
[4] Heterocycles, 2011, vol. 83, # 7, p. 1649 - 1658
[5] Patent: WO2016/7423, 2016, A1. Location in patent: Page/Page column 45
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