ChemicalBook--->CAS DataBase List--->55321-99-8

55321-99-8

55321-99-8 Structure

55321-99-8 Structure
IdentificationBack Directory
[Name]

3-HYDROXYPYRAZINE-2-CARBOXAMIDE
[CAS]

55321-99-8
[Synonyms]

Favipiravir Impurity
(3-BROMOPYRIDIN-4-...
Favipiravir intermediate
Favipiravir Desfluoro Impurity
3-HYDROXYPYRAZINE-2-CARBOXAMINE
3-Hydroxy-2-pyrazinecarboxamide
3-HYDROXYPYRAZINE-2-CARBOXAMIDE
Pyrazine-2-carboxamide, 3-hydroxy-
3-Hydroxypyrazine-2-carboxamide>
3-Hydroxypyrazine-2-carboxamide,98%
Pyrazinecarboxamide, 3,4-dihydro-3-oxo-
3,4-Dihydro-3-oxo-2-pyrazinecarboxaMide
3-Hydroxypyrazine-2-carboxylic acid amide
2-Pyrazinecarboxamide, 3,4-dihydro-3-oxo-
Pyrazinecarboxamide, 3,4-dihydro-3-oxo- (9CI)
3-HYDROXYPYRAZINE-2-CARBOXAMIDE ISO 9001:2015 REACH
[EINECS(EC#)]

202-303-5
[Molecular Formula]

C5H5N3O2
[MDL Number]

MFCD00233977
[MOL File]

55321-99-8.mol
[Molecular Weight]

139.11
Chemical PropertiesBack Directory
[Melting point ]

ca 270℃
[density ]

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

Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly), Aqueous Base (Slightly)
[form ]

Solid
[pka]

10.69±0.40(Predicted)
[color ]

Pale Brown to Brown
[λmax]

348nm(lit.)
[Stability:]

Hygroscopic
[InChI]

InChI=1S/C5H5N3O2/c6-4(9)3-5(10)8-2-1-7-3/h1-2H,(H2,6,9)(H,8,10)
[InChIKey]

SZPBAPFUXAADQV-UHFFFAOYSA-N
[SMILES]

C1(C(N)=O)=NC=CNC1=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37
[HS Code ]

29339900
Hazard InformationBack Directory
[Chemical Properties]

White crystalline powder
[Uses]

Apart from biological importance of pyridine-2-carboxamide (picolinamide, pia) as well as of its derivatives such as 3-hydroxypyridine-2-carboxamide (3-OHpia), as ligands they have found their extensive application in coordina- tion chemistry in crystal engineering .
[Synthesis Reference(s)]

Journal of the American Chemical Society, 71, p. 78, 1949 DOI: 10.1021/ja01169a023
[Synthesis]

1,2-Ethenediylbis(oxy) (9CI)

131543-46-9

2-aminopropanediamide

62009-47-6

3-HYDROXYPYRAZINE-2-CARBOXAMIDE

55321-99-8

The general procedure for the synthesis of 3-hydroxypyrazine-2-carboxamide from the compound (CAS:131543-46-9) and 2-aminomalonamide was carried out as follows: firstly, diethylaminomalonate (in the form of hydrochloric acid) was dissolved in water, and pH was adjusted by adding sodium bicarbonate to a value greater than 7. Subsequently, an extraction operation was carried out, and the organic phase was evaporated under reduced pressure. The product obtained was quantitatively converted to aminodicarbonamide by treating the product with an aqueous ammonia solution at 80 °C overnight. The product obtained in this step does not require further purification and can be directly dissolved in water for the next reaction. Next, glyoxal sodium bisulfite hemihydrate was added to this aqueous solution and the reaction mixture was stirred at 90°C for 3 hours. After completion of the reaction, the reaction mixture was adjusted to alkaline with 58% NH4OH solution. A 30% H2O2 solution was added dropwise to the rapidly stirred cold solution at 0°C. The reaction mixture was allowed to stand at room temperature to induce precipitation of 2-hydroxy-3-carboxamide pyrazine. Finally, the solid product was collected in 63% yield and purified by partial recrystallization. References: [J. Med. Chem. 1983, 26, 283-86], [J. Heterocyclic Chem. 1979, 16, 193].

[References]

[1] Patent: WO2007/144686, 2007, A1. Location in patent: Page/Page column 129-130
[2] Patent: JP5739618, 2015, B2. Location in patent: Paragraph 0024
[3] Patent: US2018/141920, 2018, A1. Location in patent: Paragraph 0215; 0216; 0217; 0218; 0219; 0220; 0221; 0222
Spectrum DetailBack Directory
[Spectrum Detail]

3-HYDROXYPYRAZINE-2-CARBOXAMIDE(55321-99-8)1HNMR
3-HYDROXYPYRAZINE-2-CARBOXAMIDE(55321-99-8)1HNMR
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