91168-58-0Relevant articles and documents
Cycloaddition Reaction of 1-Methyl-2(1H)-pyridinone with 3-(4-Ethoxyphenyl)propynenitrile - Intermediate Formation of a Spiro-oxete Ring Compound
Yadla, R.,Rao, Jampani Madhusudana,Acharya, K. R.,Tavale, S. S.,Row, T. N. Guru
, p. 1 - 2 (2007/10/02)
1-Methyl-2(1H)-pyridinone (1) reacts with 3-(4-ethoxyphenyl)propynenitrile (2) to give 1,2-dihydro-2-(4-ethoxybenzoylcyanomethylidene-1-methylpyridine (5) the structure of which is assigned based on spectral data and confirmed by X-ray.The formation of a Diels-Alder adduct is not observed.Cycloaddition at lactam carbonyl leading to the formation of a 3'-cyano-4'-(4-ethoxyphenyl)-1-methyl-1,2-dihydropyridine-2-spiro-2'-oxete (4) as an intermediate followed by valence isomerisation to give a pyridone methide derivative has been proposed.