ChemicalBook--->CAS DataBase List--->51269-81-9

51269-81-9

51269-81-9 Structure

51269-81-9 Structure
IdentificationBack Directory
[Name]

5-Chloropyridine-3-carboxylic acid methyl ester
[CAS]

51269-81-9
[Synonyms]

Methyl 5-chloronicotinate
5-Chlor-nicotinsaeure-Methylester
Methyl 5-chloropyridine-3-carboxylate
Methyl 3-chloropyridine-5-carboxylate
5-chloro-3-Pyridinecarboxylic acid methyl ester
5-Chloropyridine-3-carboxylic acid methyl ester
3-Pyridinecarboxylic acid, 5-chloro-, methyl ester
[Molecular Formula]

C7H6ClNO2
[MDL Number]

MFCD09702467
[MOL File]

51269-81-9.mol
[Molecular Weight]

171.58
Chemical PropertiesBack Directory
[Melting point ]

88-90 °C
[Boiling point ]

230.4±20.0 °C(Predicted)
[density ]

1.294±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

solid
[pka]

0.91±0.20(Predicted)
[color ]

White
[InChI]

InChI=1S/C7H6ClNO2/c1-11-7(10)5-2-6(8)4-9-3-5/h2-4H,1H3
[InChIKey]

TVUWLLCWQGXPSH-UHFFFAOYSA-N
[SMILES]

C1=NC=C(Cl)C=C1C(OC)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

5-Chloropyridine-3-carboxylic acid methyl ester(51269-81-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

5-Chloronicotinic acid

22620-27-5

5-Chloropyridine-3-carboxylic acid methyl ester

51269-81-9

Concentrated sulfuric acid (4 mL) was slowly added to a stirred solution of 5-chloronicotinic acid (5 g, 31.8 mmol) in methanol (40 mL). The reaction mixture was placed in a 75°C oil bath and heated to reflux for 12 hours. After completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove most of the methanol. The residue was diluted with distilled water (50 mL) and subsequently extracted with ethyl acetate (3 x 30 mL). The organic phases were combined and washed sequentially with saturated sodium bicarbonate solution (20 mL) and saturated sodium chloride solution (20 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure to afford methyl 5-chloronicotinate (4.4 g, 80% yield) as a white solid. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 9.08 (d, J=1.6Hz, 1H), 8.73 (d, J=2.4Hz, 1H), 8.28-8.27 (t, J=2.0Hz, 1H), 3.96 (s, 3H). Mass spectrometry (MS) showed a molecular ion peak (M+1) of 172.12.

[References]

[1] Patent: WO2015/97122, 2015, A1. Location in patent: Page/Page column 100
[2] Patent: US2014/107340, 2014, A1. Location in patent: Paragraph 0123
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 23, p. 9496 - 9508
[4] Chemische Berichte, 1928, vol. 61, p. 2211
[5] Patent: WO2009/6370, 2009, A1. Location in patent: Page/Page column 27-28
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