1,3-Dimethyl-3′,5-diphenyl-1,5-dihydro-2H,5′H-spiro[furo[2,3-d]pyrimidine-6,4′-isoxazole]-2,4,5′(3H)-trione Full article
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Molbank
ISSN: 1422-8599 |
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| Output data | Year: 2022, Volume: 2022, Number: 1, Article number : M1317, Pages count : DOI: 10.3390/m1317 | ||
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Abstract:
Michael addition–halogenation–intramolecular ring-closing (MHIRC) reactions are processes in which a halogen atom as a leaving group can attach to substrates or reactants during the reaction, which then undergoes intramolecular ring closure. In this communication the MHIRC transformation of 4-benzylidene-3-phenylisoxazol-5(4H)-one and 1,3-dimethylbarbituric acid in the presence of N-bromosuccinimide and sodium acetate in EtOH at room temperature was carefully investigated to give novel 1,3-dimethyl-3′,5-diphenyl-1,5-dihydro-2H,5′H-spiro[furo[2,3-d]pyrimi- dine-6,4′-isoxazole]-2,4,5′(3H)-trione in a good yield. The structure of the new compound was confirmed by the results of elemental analysis as well as mass, nuclear magnetic resonance, and infrared spectroscopy.
Cite:
Ryzhkova Y.E.
, Kalashnikova V.M.
, Ryzhkov F.V.
, Elinson M.N.
1,3-Dimethyl-3′,5-diphenyl-1,5-dihydro-2H,5′H-spiro[furo[2,3-d]pyrimidine-6,4′-isoxazole]-2,4,5′(3H)-trione
Molbank. 2022. V.2022. N1. M1317 . DOI: 10.3390/m1317 WOS Scopus OpenAlex
1,3-Dimethyl-3′,5-diphenyl-1,5-dihydro-2H,5′H-spiro[furo[2,3-d]pyrimidine-6,4′-isoxazole]-2,4,5′(3H)-trione
Molbank. 2022. V.2022. N1. M1317 . DOI: 10.3390/m1317 WOS Scopus OpenAlex
Identifiers:
| ≡ Web of science: | WOS:000774129900001 |
| ≡ Scopus: | 2-s2.0-85123095120 |
| ≡ OpenAlex: | W4205185764 |