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5-Hydroxypyrazine-2-carboxylic acid methyl ester

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5-Hydroxypyrazine-2-carboxylic acid methyl ester Basic information

Product Name:
5-Hydroxypyrazine-2-carboxylic acid methyl ester
Synonyms:
  • CBI-BB ZERO/008486
  • 5-HYDROXY-PYRAZINE-2-CARBOXYLIC ACID METHYL ESTER
  • METHYL 5-HYDROXYPYRAZINE-2-CARBOXYLATE
  • 5-HYDROXY-PYRAZINE-2-CARBOXYLIC ACID METHYL ESTER 95%
  • Methyl 5-oxo-4,5-dihydro-2-pyrazinecarboxylate
  • Methyl 5-hydropyrazine-2-carboxylate
  • 5-Hydrocy-pyrazine-2-carboxylic acid methyl ester
  • 2-Hydroxy-5-(methoxycarbonyl)pyrazine, 2-Hydroxy-5-(methoxycarbonyl)-1,4-diazine
CAS:
13924-95-3
MF:
C6H6N2O3
MW:
154.12
EINECS:
1312995-182-4
Product Categories:
  • Heterocycles
  • Pyrazine
Mol File:
13924-95-3.mol
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5-Hydroxypyrazine-2-carboxylic acid methyl ester Chemical Properties

Melting point:
183-185 °C
Density 
1.39
storage temp. 
Sealed in dry,Room Temperature
pka
10.55±0.40(Predicted)
Appearance
White to light brown Solid
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Safety Information

HS Code 
2933998090
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5-Hydroxypyrazine-2-carboxylic acid methyl ester Usage And Synthesis

Uses

5-Hydroxypyrazine-2-carboxylic Acid Methyl Ester is a metabolite of Pyrazinamide (P840600), an antibacterial (tuberculostatic).

Synthesis

67-56-1

34604-60-9

13924-95-3

General procedure for the synthesis of methyl 5-hydroxypyrazine-2-carboxylate from methanol and 5-oxo-4,5-dihydropyrazine-2-carboxylic acid: Acetyl chloride (152 mL, 2.08 mol) was slowly added dropwise to methanol (5 L) at -20 °C. After the dropwise addition was completed, stirring was continued at this temperature for 30 minutes. Subsequently, 5-hydroxypyrazine-2-carboxylic acid (100 g, 714 mmol) was added and the mixture was heated to reflux and the reaction was maintained for 2 hours. Upon completion of the reaction, the solvent was removed by vacuum concentration and the residue was recrystallized from methanol (400 mL) to give 71 g (464 mmol) of methyl 5-hydroxypyrazine-2-carboxylate in 65% yield.

References

[1] Patent: WO2013/14567, 2013, A1. Location in patent: Page/Page column 80-81
[2] Patent: EP2239253, 2010, A1. Location in patent: Page/Page column 96
[3] Patent: EP1452525, 2004, A1. Location in patent: Page 15

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