20364-37-8Relevant articles and documents
N-3-oxoalkylamides and -thioamides in the synthesis of heterocyclic compounds. 7*. Study of the cyclization of N-(3-oxoalkyl)amides of tosylacetic acid
Fisyuk,Poendaev
, p. 895 - 900 (2007/10/03)
Alkyl-substituted N-(3-oxoalkyl)amides of tosylacetic acid are cyclized under the action of bases with the formation of 3-tosyl-3,6-dihydropyridin-2(1H) -ones. In the presence of a phenyl substituent at position C(1) of the 3-oxoalkyl chain the
Process for the production of 6-substituted 4-methyl-2-pyridones
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, (2008/06/13)
Process for the production of 6-substituted-4-methyl-2-pyridones having the formula: STR1 wherein R is a branched or unbranched alkyl group, a halogenated branched or unbranched alkyl group or a substituted or unsubstituted aryl group. Senecioic acid amide having the formula: STR2 is reacted in a solvent at an elevated temperature in the presence of a Lewis acid (as a catalyst) with an acyl chloride having the formula: STR3 wherein R has the same meaning as above. The reaction mixture is subsequently placed in an aqueous phase for hydrolysis. The 6-substituted-4-methyl-2-pyridone is separated by extraction through the buffering of the reaction mixture at a pH of 4 to 5.
On the knowledge of acetylenecarboxylic acids. 14. alpha-Pyrone from 3-hydroxy-4-alkynoic acid esters.
SCHULTE,REISCH,HEINE
, p. 234 - 239 (2007/10/07)
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