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20737-42-2

20737-42-2 Structure

20737-42-2 Structure
IdentificationMore
[Name]

2-HYDROXY-3-PYRAZINECARBOXYLIC ACID
[CAS]

20737-42-2
[Synonyms]

2-Carboxy-3-hydroxypyrazine
3-Hydroxypyrazine-2-carbo...
3-Hydroxypyrazinecarboxylic acid
2-oxo-1H-pyrazine-3-carboxylicaci
2-oxo-1H-pyrazine-3-carboxylic acid
3-HYDROXYPYRAZINE-2-CARBOXYLIC ACID
2-HYDROXY-3-PYRAZINECARBOXYLIC ACID
3-Hydroxy-2-pyrazinecarboxylic acid
3-hydroxy-2-piperazinecarboxylic acid
3-HYDROXY-PIPERAZINE-2-CARBOXYLIC ACID
3-Hydroxypyrazine-2-carboxylic acid 97%
2-Pyrazinecarboxylicacid, 3,4-dihydro-3-oxo
3-Oxo-3,4-dihydropyrazine-2-carboxylic acid
3-hydroxy-2-pyrazinecarboxylic acid(SALTDATA: FREE)
2-HYDROXY-3-PYRAZINECARBOXYLIC ACID ISO 9001:2015 REACH
[Molecular Formula]

C5H4N2O3
[MDL Number]

MFCD00235136
[Molecular Weight]

140.1
[MOL File]

20737-42-2.mol
Chemical PropertiesBack Directory
[Melting point ]

218-220 °C
[density ]

1.63±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

12.72±0.20(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C5H4N2O3/c8-4-3(5(9)10)6-1-2-7-4/h1-2H,(H,7,8)(H,9,10)
[InChIKey]

FJZRUSFQHBBTCC-UHFFFAOYSA-N
[SMILES]

C1(C(O)=O)=NC=CNC1=O
[CAS DataBase Reference]

20737-42-2(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319
[Precautionary statements ]

P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2-HYDROXY-3-PYRAZINECARBOXYLIC ACID(20737-42-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Aminopyrazine-2-carboxylic acid

5424-01-1

2-HYDROXY-3-PYRAZINECARBOXYLIC ACID

20737-42-2

Example 4: Synthesis of 3-[3-(5-chloro-1H-benzimidazol-2-yl)-azetidin-1-yl]-pyrazine-2-carboxylic acid Step 1. Preparation of 3-hydroxypyrazine-2-carboxylic acid: 3-aminopyrazine-2-carboxylic acid (6.95 g, 0.05 mol) was dissolved in a mixed solution of water (55 mL) and sulfuric acid (55 mL, 3.75 M) and heated to 50 °C. Sodium nitrite solution (18.5 mL, 0.06 mol) was slowly added to this solution and the reaction mixture was subsequently cooled to 12 °C. During the addition, the reaction temperature was maintained in the range of 10-16 °C for 30 minutes. Afterwards, the mixture was heated to boiling over 30 minutes. After completion of the reaction, it was cooled to room temperature and filtered to collect the yellow solid. The resulting solid was dissolved in dilute sodium bicarbonate solution, acidified with 10% hydrochloric acid to precipitate the carboxylic acid product and collected by filtration. The crude product was purified by recrystallization from water to give a yellow-orange crystalline solid (4.1 g, 58% yield).

[References]

[1] Synthetic Communications, 2010, vol. 40, # 20, p. 2988 - 2999
[2] Patent: WO2011/143129, 2011, A1. Location in patent: Page/Page column 62
[3] Journal of Heterocyclic Chemistry, 1997, vol. 34, # 1, p. 27 - 32
[4] Patent: WO2013/169907, 2013, A1. Location in patent: Page/Page column 44; 45
[5] MedChemComm, 2015, vol. 6, # 7, p. 1311 - 1317
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