143082-98-8Relevant articles and documents
FIVE-MEMBERED 2,3-DIOXOHETEROCYCLES. XXXVII. REACTION OF 3-AROYL-1,2-DIHYDRO-4H-PYRROLOBENZOXAZINE-1,2,4-TRIONES WITH ALKYL- AND ARYLAMINES
Maslivets, A. N.,Mashevskaya, I. V.,Andreichikov, Yu. S.
, p. 1709 - 1715 (2007/10/02)
3-Aroyl-1,2-dihydro-4H-pyrrolobenzoxazine-1,2,4-triones react with an equivalent amount of alkyl- and arylamines with the formation of N-substituted 3a-amino-3-aroyl-2-hydroxy-1,3a-dihydro-4H-pyrrolobenzoxazine-1,4-diones and N-substituted 4-aryl-2,4-dioxo-(Z)-3-(2-oxo-3,4-dihydro-2H-1,4-benzoxazin-3-ylidene)butyramides, which in the case of alkylamines exist as the ring isomers (Z)-3-(1-alkyl-5-aryl-5-hydroxy-2,3-dioxotetrahydro-4-pyrrolylidene)-3,4-dihydro-2H-1,4-benzoxazin-2-ones.An excess of the amine leads to the formation of (Z)-3-phenacylidene-3,4-dihydro-2H-1,4-benzoxazin-2-ones and substituted oxamides.
RECYCLIZATION OF METHYL-4-HYDROXY-2-(o-HYDROXYPHENYLAMINO)-5-OXO-2,5-DIHYDROPYRROLE-2-CARBOXYLATE INTO THE AMIDE OF (2-OXO-3,4-DIHYDRO-2H-1,4-BENZOXAZIN-3-YLIDENE)PYRUVIC ACID
Maslivets, A. N.,Smirnova, L. I.,Andreichikov, Yu. S.
, p. 1154 (2007/10/02)
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