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1256789-39-5

1256789-39-5 Structure

1256789-39-5 Structure
IdentificationBack Directory
[Name]

Methyl 4-broMo-6-Methoxypyridine-2-carboxylate
[CAS]

1256789-39-5
[Synonyms]

Methyl 4-bromo-6-methoxypicolinate
Methyl 4-broMo-6-Methoxypyridine-2-carboxylate
2-Pyridinecarboxylic acid, 4-bromo-6-methoxy-, methyl ester
[Molecular Formula]

C8H8BrNO3
[MDL Number]

MFCD18257508
[MOL File]

1256789-39-5.mol
[Molecular Weight]

246.06
Chemical PropertiesBack Directory
[storage temp. ]

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

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 4-broMo-6-Methoxypyridine-2-carboxylate(1256789-39-5)1HNMR
Methyl 4-broMo-6-Methoxypyridine-2-carboxylate(1256789-39-5)1HNMR
Methyl 4-broMo-6-Methoxypyridine-2-carboxylate(1256789-39-5)13CNMR
Hazard InformationBack Directory
[Synthesis]

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

1443759-42-9

Methyl 4-broMo-6-Methoxypyridine-2-carboxylate

1256789-39-5

General procedure for the synthesis of methyl 4-bromo-6-methoxypyridine-2-carboxylate from methyl 4-amino-6-methoxypyridine-2-carboxylate: To a 120 mL solution of acetonitrile containing 3.47 mL (29.3 mmol) of tert-butyl nitrite and 6.60 g (29.3 mmol) of copper(II) bromide, add slowly and dropwise at 40 °C 3.33 g (18.3 mmol) of methyl 4-amino-6-methoxypyridine-2-carboxylate dissolved in 30 mL of acetonitrile. The reaction mixture was stirred at 80 °C for 1 h and then poured into ice water. The precipitate was collected by filtration, washed with water and dried. The crude product was purified by fast chromatography (petroleum ether/ethyl acetate = 4/1 → 3/1) to give 2.50 g (56% yield) of the target product. eSI-MS: m/z = 246 (M + H)+.

[References]

[1] Patent: WO2013/87805, 2013, A1. Location in patent: Page/Page column 76
[2] Patent: US2013/158042, 2013, A1. Location in patent: Paragraph 0497; 0498; 0499; 0500
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