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6′-Amino-5,7-dibromo-2-oxo-3′-(trifluoromethyl)-1′H-spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-5′-carbonitrile Full article

Journal Molbank
ISSN: 1422-8599
Output data Year: 2021, Volume: 2022, Number: 1, Article number : M1309, Pages count : DOI: 10.3390/m1309
Authors Ryzhkova Yuliya E. 1 , Kalashnikova Varvara M. 1 , Elinson Michail N. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prospekt, 119991 Moscow, Russia

Abstract: The multicomponent reactions are environmentally benign synthetic methods of building-up of complex molecules and several levels of structural diversity for diverse applications. Spirooxindoles are an important synthetic target possessing extended biological activity and drug discovery applications. In this communication, the multicomponent transformation of 5,7-dibromoisatin, malononitrile, and 5-(trifluoromethyl)-2,4-dihydro-3H-pyrazol-3-one in EtOH at reflux in the presence of sodium acetate was carefully investigated to give 6′-amino-5,7-dibromo-2-oxo-3′-(trifluoromethyl)-1′H-spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-5′-carbonitrile in excellent yield. The structure of the new compound was established by means of elemental analysis, mass and nuclear magnetic resonance, and infrared spectroscopy.
Cite: Ryzhkova Y.E. , Kalashnikova V.M. , Elinson M.N.
6′-Amino-5,7-dibromo-2-oxo-3′-(trifluoromethyl)-1′H-spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-5′-carbonitrile
Molbank. 2021. V.2022. N1. M1309 . DOI: 10.3390/m1309 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000774148300001
≡ Scopus: 2-s2.0-85121835932
≡ OpenAlex: W4200129629
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