ChemicalBook--->CAS DataBase List--->1210419-26-3

1210419-26-3

1210419-26-3 Structure

1210419-26-3 Structure
IdentificationBack Directory
[Name]

Methyl 6-bromo-5-fluoropyridine-2-carboxylate
[CAS]

1210419-26-3
[Synonyms]

uoropicoL
6-bromo-5-fL
methyl 6-bromo-5-fluoropicolinat
Methyl 6-bromo-5-fluoropicolinate
N'-(3,4-dichlorophenyl)ethane-1,6-diamine
Methyl 6-bromo-5-fluoropyridine-2-carboxylate
6-Bromo-5-fluoro-pyridine-2-carboxylic acid methyl ester
2-Pyridinecarboxylic acid, 6-bromo-5-fluoro-, methyl ester
Methyl 6-bromo-5-fluoropicolinate, 2-Bromo-3-fluoro-6-(methoxycarbonyl)pyridine
[Molecular Formula]

C7H5BrFNO2
[MDL Number]

MFCD14698111
[MOL File]

1210419-26-3.mol
[Molecular Weight]

234.02
Chemical PropertiesBack Directory
[Boiling point ]

275.5±35.0 °C(Predicted)
[density ]

1.660±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

-3.45±0.10(Predicted)
[color ]

white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H227
[Precautionary statements ]

P501-P210-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P403+P235
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 6-bromo-5-fluoropyridine-2-carboxylate(1210419-26-3)1HNMR
Methyl 6-bromo-5-fluoropyridine-2-carboxylate(1210419-26-3)1HNMR
Methyl 6-bromo-5-fluoropyridine-2-carboxylate(1210419-26-3)19FNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

6-Bromo-5-fluoro-2-pyridinecarboxylic acid

1052714-46-1

Methyl 6-bromo-5-fluoropyridine-2-carboxylate

1210419-26-3

Synthesis of methyl 6-bromo-5-fluoro-pyridinecarboxylate: Concentrated sulfuric acid (4.2 eq.) was slowly added to a methanol (0.2 M) solution of 6-bromo-5-fluoro-2-pyridinecarboxylic acid (1.0 eq.) and the reaction mixture was stirred at room temperature. The progress of the reaction was monitored by LC/MS and the reaction was completed after about 2 hours. The reaction mixture was diluted with ethyl acetate and saturated aqueous sodium bicarbonate solution was added slowly to quench the reaction. The mixture was transferred to a partition funnel and extracted with ethyl acetate. The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford methyl 6-bromo-5-fluoropyridinecarboxylate as a white solid (yield >99%). The product was characterized by LC/MS: m/z = 233.9/235.9 ([M+H]+), retention time Rt = 0.69 min.

[References]

[1] Patent: US2010/56576, 2010, A1. Location in patent: Page/Page column 48
[2] Patent: WO2012/4217, 2012, A1. Location in patent: Page/Page column 65-66
[3] Patent: US2012/225062, 2012, A1. Location in patent: Page/Page column 26; 27
[4] Patent: US2012/225061, 2012, A1. Location in patent: Page/Page column 22
[5] Patent: WO2013/175388, 2013, A1. Location in patent: Page/Page column 44
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