ChemicalBook--->CAS DataBase List--->768-05-8

768-05-8

768-05-8 Structure

768-05-8 Structure
IdentificationMore
[Name]

Pyrazinoic acid hydrazide
[CAS]

768-05-8
[Synonyms]

AKOS BBS-00004101
PYRAZINE-2-CARBOXYLIC ACID HYDRAZIDE
Pyrazin-2-carbohydrazide
Pyrazinecarboxylic acid, hydrazide (7CI,8CI,9CI)
PYRAZINE-2-CARBOHYDRAZIDE
PYRAZINOIC ACID HYDRAZIDE
[Molecular Formula]

C5H6N4O
[MDL Number]

MFCD00778762
[Molecular Weight]

138.13
[MOL File]

768-05-8.mol
Chemical PropertiesBack Directory
[Melting point ]

169 °C
[density ]

1.335±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

10.07±0.10(Predicted)
[Appearance]

Light yellow to light brown Solid
[CAS DataBase Reference]

768-05-8(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P280-P302+P352-P312-P322-P363-P501
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

Pyrazinoic acid hydrazide(768-05-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

METHYL PYRAZINE-2-CARBOXYLATE

6164-79-0

Pyrazinoic acid hydrazide

768-05-8

The general procedure for the synthesis of pyrazine-2-carboxylic acid methyl ester as a raw material for the synthesis of pyrazine-2-carbohydrazide was as follows: to a stirred solution of methyl pyrazine-2-carboxylic acid methyl ester (11.1 g, 80 mmol) dissolved in 140 mL of ethanol (EtOH) was slowly added hydrazine hydrate (15.6 mL, 320 mmol). The reaction mixture was heated to reflux and kept for 2 hours. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the resulting residue was dried under high vacuum to afford the title compound pyrazine-2-carbohydrazide (11.1 g, 100% yield) as a white solid. The product can be used directly in the subsequent reaction steps without further purification.

[References]

[1] Patent: WO2005/16909, 2005, A1. Location in patent: Page/Page column 73
[2] Patent: WO2005/66163, 2005, A2. Location in patent: Page/Page column 128
[3] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 14, p. 5007 - 5015
[4] European Journal of Inorganic Chemistry, 2011, # 32, p. 5036 - 5042
[5] European Journal of Medicinal Chemistry, 2009, vol. 44, # 12, p. 4954 - 4959
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