27074-03-9

Usage

Uses

2-Hydroxy-1,4-dimethyl-5-cyano-6-pyridinon is used in the synthesis of many azo dyes.

InChI:InChI=1/C8H8N2O2/c1-5-3-7(11)10(2)8(12)6(5)4-9/h3,11H,1-2H3

Upstream product

• 141-97-9 ethyl acetoacetate 
• 105-56-6 ethyl 2-cyanoacetate 
• 74-89-5 methylamine 
• 105-34-0 methyl 2-cyanoacetate 
• 105-45-3 acetoacetic acid methyl ester 
• 6330-25-2 N-methyl-2-cyanoacetamide 

Downstream Products

• 85843-03-4 6-hydroxy-1,4-dimethyl-5-(4-morpholinylmethyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile 
• 85843-04-5 6-hydroxy-1,4-dimethyl-5-(4-phenyl-1-piperazinylmethyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile 
• 75511-98-7 1,2-dihydro-1,4-dimethyl-6-hydroxy-2-oxo-5-phenylazopyridine-3-carbonitrile 
• 72570-56-0 3-Methyl-1-oxo-1H,5H-pyrido<1,2-a>benzimidazole 
• 329348-61-0 6-Chloro-3-cyano-5-formyl-1,4-dimethylpyridin-2(1H)-one 
• 59312-61-7 disperse yellow 114 

Relevant academic research and scientific papers

An Efficient Method for the Synthesis of 3-Cyano-6-hydroxy-2(1H)- pyridinones under Microwave Irradiation and Solvent-free Conditions

Three component condensation of alkylacetoacetates, primary amines, and alkyl cyanoacetates catalyzed by solid supports under microwave irradiation gave N-alkyl 3-cyano-6-hydroxy-2(1H)-pyridinones with high yields. Upon carrying out the reaction under the same condition on acidic alumina, zeolite HY, silica gel, and montmorillonite K-10, the best yields were achieved by silica gel.

Synthesis of Some Mannich Bases of Substituted Glutaconimides as Anticonvulsant Agents

Mannich reactions on substituted glutaconimides (I) and (II) furnish the Mannich bases (III-V).All the compounds are found to be devoid of any anticonvulsant activity.

Azo pyridone dyestuffs containing at least one reactive phosphoric or phosphonic acid group

Azo pyridone dyestuffs containing at least one reactive phosphoric or phosphonic acid group. The dyestuffs are characterized by the formula: wherein A is an aromatic radical containing at least one phosphoric or phosphonic acid group and R is a monovalent radical derived from a pyridone coupling component by removing a hydrogen atom attached to a ring carbon atom of the pyridone ring. The aromatic radical A is preferably a phenyl or naphthyl group. In addition to its phosphonic or phosphoric acid group or groups, radical A may be substituted with one or more halogen, alkyl, alkoxy, nitro, sulfonic acid or carboxylic acid groups. Cellulosic textiles, e.g., cotton or cotton/polyester blends, may be reactively dyed with these dyestuffs in an acid, neutral or alkaline bath using dicyandiamide or the equivalent. The phosphoric or phosphonic acid groups and the cellulosic material react to fix the dye through an ester linkage. Examples of suitable dyestuffs include those having the formula: STR1 and STR2

Water-insoluble monoazo pyridine dyes

Water-insoluble monoazo dyes of the formula SPC1 Produced by reacting a diazotized amine of the benzene, naphthalene, diphenyl, diphenylmethane or heterocyclic series which is free from water solubilizing groups with the appropriate 6-hydroxy-2-pyridone and the utility thereof for the dyeing and printing of synthetic fabric materials to yellow to red shades having excellent fastness to light and sublimation.