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72716-80-4

72716-80-4 Structure

72716-80-4 Structure
IdentificationBack Directory
[Name]

5,6-DIMETHYL-2-OXO-1,2-DIHYDRO-PYRIDINE-3-CARBONITRILE
[CAS]

72716-80-4
[Synonyms]

104166
3-Cyano-5,6-diMethylpyrid-2-one
3-Cyano-5,6-diMethylpyridin-2-ol
2-Hydroxy-5,6-dimethylnicotinonitrile
2-Hydroxy-3-cyano-5,6-diMethylpyridine
2-Hydroxy-5,6-dimethyl-3-pyridinecarbonitrile
2-HYDROXY-5,6-DIMETHYLPYRIDINE-3-CARBONITRILE
1,2-dihydro-5,6-diMethyl-2-oxo-3-Pyridinecarbonitrile
1,2-dihydro-5,6-dimethyl-2-oxopyridine-3-carbonitrile
5,6-Dimethyl-2-oxo-1,2-dihydro-3-pyridinecarbonitrile
5,6-DIMETHYL-2-OXO-1,2-DIHYDRO-PYRIDINE-3-CARBONITRILE
3-Pyridinecarbonitrile, 1,2-dihydro-5,6-diMethyl-2-oxo-
3-Pyridinecarbonitrile,1,2-dihydro-5,6-dimethyl-2-oxo-(9CI)
5,6-DIMETHYL-2-OXO-1,2-DIHYDRO-PYRIDINE-3-CARBONITRILE ISO 9001:2015 REACH
[Molecular Formula]

C8H8N2O
[MDL Number]

MFCD03004855
[MOL File]

72716-80-4.mol
[Molecular Weight]

148.16
Chemical PropertiesBack Directory
[Melting point ]

270 °C
[Boiling point ]

335.6±35.0 °C(Predicted)
[density ]

1.16±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

Acetic Acid, DMSO
[pka]

9.44±0.10(Predicted)
[Appearance]

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P280-P305+P351+P338-P310
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

An intermediate in the preparation of HIV-1 specific reverse transcriptase inhibitors, antiallergic agents, and Omeprazole metabolites.
[Synthesis Reference(s)]

Journal of Heterocyclic Chemistry, 24, p. 351, 1987 DOI: 10.1002/jhet.5570240211
[Synthesis]

3-Buten-2-one, 4-hydroxy-3-methyl-, sodium salt (1:1)

143193-92-4

2-Cyanoacetamide

107-91-5

5,6-DIMETHYL-2-OXO-1,2-DIHYDRO-PYRIDINE-3-CARBONITRILE

72716-80-4

The general procedure for the synthesis of 2-hydroxy-3-cyano-5,6-dimethylpyridine from the compound (CAS:143193-92-4) and cyanoacetamide was as follows: sodium (E/Z)-2-methyl-3-oxo-1-en-1-ol (77.6 g, 0.64 mol) was added to 480 mL of water, followed by the addition of cyanoacetamide (49.0 g, 0.70 mol). To the mixture was added a piperidine-acetic acid solution prepared from acetic acid (9.16 g, 8.75 mL, 0.15 mol), 21.2 mL of water and pyridine (13.0 g, 15.1 mL, 0.15 mol). The mixture was heated at reflux for 4 hours and then stirred at room temperature for 16 hours. Upon completion of the reaction, acetic acid (75.5 g, 72 mL, 1.26 mol) was added to the reaction mixture, prompting the precipitation of a pale yellow solid. The precipitate was collected by diafiltration, washed with water and dried under reduced pressure at 55 °C for 2 hours. A final 66.4 g (70% of theoretical yield) of light yellow solid product was obtained.

[References]

[1] Patent: CN105530814, 2016, A. Location in patent: Paragraph 0328; 0329; 0330
[2] Journal of Heterocyclic Chemistry, 1987, vol. 24, p. 351 - 355
Spectrum DetailBack Directory
[Spectrum Detail]

5,6-DIMETHYL-2-OXO-1,2-DIHYDRO-PYRIDINE-3-CARBONITRILE(72716-80-4)1HNMR
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