5-Hydroxypyrazine-2-carboxylic acid methyl ester
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
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
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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