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51171-02-9

51171-02-9 Structure

51171-02-9 Structure
IdentificationBack Directory
[Name]

methyl 3-bromopyrazine-2-carboxylate
[CAS]

51171-02-9
[Synonyms]

Methyl 3-bromopyrazine-2-carbo
methyl 3-bromopyrazine-2-carboxylate
Methyl 2-bromopyrazine-3-carboxylate
Methyl 3-BroMo-2-pyrazinecarboxylate
Methyl 3-bromopyrazine-2-carboxylate 96%
3-bromo-2-Pyrazinecarboxylic acid methyl ester
2-Bromopyrazine-3-carboxylic acid methyl ester
Pyrazinecarboxylic acid, 3-bromo-, methyl ester
3-BroMo-pyrazine-2-carboxylic acid Methyl ester
2-Pyrazinecarboxylic acid, 3-bromo-, methyl ester
methyl 3-bromopyrazine-2-carboxylate ISO 9001:2015 REACH
[Molecular Formula]

C6H5BrN2O2
[MDL Number]

MFCD08753935
[MOL File]

51171-02-9.mol
[Molecular Weight]

217.03
Chemical PropertiesBack Directory
[Melting point ]

44℃
[Boiling point ]

264.7±35.0℃ (760 Torr)
[density ]

1.669±0.06 g/cm3 (20 ºC 760 Torr)
[Fp ]

113.9±25.9℃
[storage temp. ]

2-8°C
[form ]

solid
[pka]

-2.41±0.10(Predicted)
[color ]

Off-white to grey
[InChI]

InChI=1S/C6H5BrN2O2/c1-11-6(10)4-5(7)9-3-2-8-4/h2-3H,1H3
[InChIKey]

CMITUAXQMWSHLL-UHFFFAOYSA-N
[SMILES]

C1(C(OC)=O)=NC=CN=C1Br
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 3-bromopyrazine-2-carboxylate(51171-02-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 3-amino-2-pyrazinecarboxylate

16298-03-6

methyl 3-bromopyrazine-2-carboxylate

51171-02-9

General procedure for the synthesis of methyl methyl 3-bromopyrazine-2-carboxylate from methyl 3-aminopyrazine-2-carboxylate: bromine (3.91 g, 24.46 mmol) was added slowly and dropwise at 0 °C to a stirred mixture containing methyl 3-aminopyrazine-2-carboxylate (1.27 g, 8.29 mmol) and hydrobromic acid (4.70 mL, 41.5 mmol). . Subsequently, a solution of sodium nitrite (1.44 g, 20.9 mmol) dissolved in water (6 mL) was added dropwise. The reaction mixture was continued to be stirred at 0 °C for 15 min. Upon completion of the reaction, the pH was adjusted to 8 with saturated aqueous sodium bicarbonate solution, followed by extraction with ethyl acetate (80 mL) and chloroform (50 mL). The organic phases were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure to afford 1.13 g (63% yield) of an orange oil, which solidified to the target product, methyl methyl-3-bromopyrazine-2-carboxylate, upon standing.

[References]

[1] Patent: WO2006/91506, 2006, A2. Location in patent: Page/Page column 47
[2] Patent: WO2006/49681, 2006, A2. Location in patent: Page/Page column 45-46
[3] Patent: WO2006/121588, 2006, A2. Location in patent: Page/Page column 51
[4] Patent: WO2006/121860, 2006, A2. Location in patent: Page/Page column 51
[5] Patent: WO2006/121904, 2006, A1. Location in patent: Page/Page column 51
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