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959616-64-9

959616-64-9 Structure

959616-64-9 Structure
IdentificationBack Directory
[Name]

Methyl 2-chloro-5-fluoro-6-methoxynicotinate
[CAS]

959616-64-9
[Synonyms]

Methyl 2-chloro-5-fluoro-6-methoxynicotinate
2-Chloro-5-fluoro-6-methoxy-nicotinic acid methyl ester
Methyl 2-chloro-5-fluoro-6-methoxy-pyridine-3-carboxylate
Methyl 2-chloro-5-fluoro-6-methoxynicotinate ISO 9001:2015 REACH
3-Pyridinecarboxylic acid, 2-chloro-5-fluoro-6-methoxy-, methyl ester
Methyl 2-chloro-5-fluoro-6-methoxypyridine-3-carboxylate, 2-Chloro-5-fluoro-6-methoxy-3-(methoxycarbonyl)pyridine
[Molecular Formula]

C8H7ClFNO3
[MDL Number]

MFCD12025844
[MOL File]

959616-64-9.mol
[Molecular Weight]

219.597
Chemical PropertiesBack Directory
[Melting point ]

66-68°
[Boiling point ]

279.8±40.0 °C(Predicted)
[density ]

1.366±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-3.47±0.10(Predicted)
[Appearance]

white solid
[InChI]

InChI=1S/C8H7ClFNO3/c1-13-7-5(10)3-4(6(9)11-7)8(12)14-2/h3H,1-2H3
[InChIKey]

KGWMUWXJNVKKCF-UHFFFAOYSA-N
[SMILES]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 2-chloro-5-fluoro-6-methoxynicotinate(959616-64-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

METHYL 2,6-DICHLORO-5-FLUORONICOTINATE

189281-66-1

Sodium Methoxide

124-41-4

Methyl 2-chloro-5-fluoro-6-methoxynicotinate

959616-64-9

Intermediate 73b: Synthesis of methyl 2-chloro-5-fluoro-6-methoxypyridine-3-carboxylate. Sodium methanol (1.86 mL, 11.91 mmol) was added to a solution of toluene (9 mL) containing methyl 2,6-dichloro-5-fluoropyridine-3-carboxylate (1.8 g, 8.03 mmol), and the reaction mixture was stirred for 1 h at room temperature. After completion of the reaction, ethyl acetate (20 mL) and water (20 mL) were added to the mixture to separate the organic and aqueous layers. The aqueous layer was extracted with ethyl acetate (3 x 20 mL), the organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target product methyl 2-chloro-5-fluoro-6-methoxypyridine-3-carboxylate (1.72 g, 7.83 mmol, 97% yield) as an orange solid. The product was confirmed by 1H NMR (CDCl3, 400 MHz): δ 7.92 (1H, d, J = 9.6 Hz), 4.09 (3H, s), 3.92 (3H, s). Mass spectrometry analysis (Method 2): retention time 1.71 min, m/z 220.0 [M + H]+.

[References]

[1] Patent: WO2016/51193, 2016, A1. Location in patent: Paragraph 00667; 00670; 00671
[2] Patent: EP2022793, 2009, A1. Location in patent: Page/Page column 72
[3] Patent: EP2022793, 2009, A1. Location in patent: Page/Page column 72
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