Reaction of benzocaine with indane-1,3-dione-2-carbaldehyde afforded the corresponding azomethine. Ethoxymethylenemalonate reacted with benzocaine to form ethyl 4-{[2-(ethoxycarbonyl)-4-methoxy-3-oxobuten-1-yl]amino}benzoate, which was converted to the corresponding quinolone when heated to 185-190A degrees C. Reactions of benzocaine with aliphatic aldehydes furnished 2,3-alkyl-substituted quinolines.
作者:Yu. A. Azev、O. S. Ermakova、V. S. Berseneva、V. A. Bakulev
DOI:10.1134/s1070363216110074
日期:2016.11
Reaction of benzocaine with indane-1,3-dione-2-carbaldehyde afforded the corresponding azomethine. Ethoxymethylenemalonate reacted with benzocaine to form ethyl 4-[2-(ethoxycarbonyl)-4-methoxy-3-oxobuten-1-yl]amino}benzoate, which was converted to the corresponding quinolone when heated to 185-190A degrees C. Reactions of benzocaine with aliphatic aldehydes furnished 2,3-alkyl-substituted quinolines.