ChemicalBook--->CAS DataBase List--->204378-37-0

204378-37-0

204378-37-0 Structure

204378-37-0 Structure
IdentificationBack Directory
[Name]

Methyl 4-chloro-6-Methoxypicolinate
[CAS]

204378-37-0
[Synonyms]

Regorafenib Impurity 125
Levocarnitine Impurity 49
Methyl 4-chloro-6-Methoxypicolinate
2-Pyridinecarboxylic acid, 4-chloro-6-methoxy-, methyl ester
[Molecular Formula]

C8H8ClNO3
[MDL Number]

MFCD18257705
[MOL File]

204378-37-0.mol
[Molecular Weight]

201.61
Chemical PropertiesBack Directory
[Boiling point ]

290.8±35.0 °C(Predicted)
[density ]

1.288±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-1.53±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 4-chloro-6-Methoxypicolinate(204378-37-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

methyl 4-amino-6-methoxypyridine-2-carboxylate

1443759-42-9

Methyl 4-chloro-6-Methoxypicolinate

204378-37-0

General procedure for the synthesis of methyl 4-chloro-6-methoxypyridine-2-carboxylate from methyl 4-amino-6-methoxy-pyridine-2-carboxylate: to a mixture of 1.25 mL (10.5 mmol) of tert-butyl nitrite and 1.42 g (10.5 mmol) of copper(II) chloride in 40 mL of acetonitrile was added slowly, dropwise, at 40 °C, 1.20 g (6.59 mmol) of 4- methyl amino-6-methoxy-pyridine-2-carboxylate dissolved in 10 mL of acetonitrile. The reaction mixture was stirred at 80 °C for 1 h and then poured into ice water, acidified with 4 M aqueous HCl and extracted with EtOAc. The combined organic phases were dried with anhydrous sodium sulfate, filtered and concentrated in vacuum. The crude product was purified by fast chromatography (eluent ratio: petroleum ether/EtOAc 3/1→2/1). A product of 650 mg was obtained in 49% yield. eSI-MS: m/z = 202 (M + H)+. hPLC retention time: 1.12 min (Method 5).

[References]

[1] Patent: WO2013/87805, 2013, A1. Location in patent: Page/Page column 75
[2] Patent: US2013/158042, 2013, A1. Location in patent: Paragraph 0477; 0478; 0479; 0480; 0481
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