Reaction of 2-cyano-3-(4,5-dibromo-2-furyl)-2-propenenitrile and methyl 2-cyano-3-(4,5-dibromo-2-furyl)-2-propenoate with nucleophiles

Autor:	Viera Knoppová, Rudolf Kada, Pavel Čepec, Jaroslav Kováč
Rok vydání:	1984
Předmět:	2-Propenenitrile biology Chemistry Kinetics General Chemistry Medicinal chemistry chemistry.chemical_compound Sulfonate Nucleophile biology.protein Nucleophilic substitution Organic chemistry Piperidine Methanol Organic anion
Zdroj:	Collection of Czechoslovak Chemical Communications. 49:984-991
ISSN:	1212-6950 0010-0765
Popis:	Methyl 2-cyano-3-(4-bromo-5-R-X-2-furyl)-2-propenenitriles and 2-propenoates were prepared from 2-cyano-3-(4,5-dibromo-2-furyl)-2-propenenitrile and methyl 2-cyano-3-(4,5-dibromo-2-furyl)-2-propenoate and the respective nucleophiles R-XNa (X = S, R = C6H5, 2-benzimidazolyl, 2-benzothiazolyl, 2-pyrimidinyl, and X = SO2, R = C6H5). The same products also originate by condensation of 4-bromo-5-R-X-2-furaldehydes with malononitrile or methyl cyano acetate under catalysis of alcoholates. Bis(3-bromo-5-formyl-2,2'-furyl) sulfide and bis(5-formyl-2,2'-furyl) sulfide were prepared from 4-X-5-bromo-2-furaldehydes (X = H, Br) with sodium sulfide. 4-Bromo-5-X-2-furaldehydes (X = H, Br) react with sodium hydrogen selenide to give bis-(3-bromo-5-formyl-2,2'-furyl)- or bis(5-formyl-2,2'-furyl) selenides. 2-Cyano-3-(4-bromo-5-amino-2-furyl)-2-propenenitrile and methyl 2-cyano-3-(4-bromo-5-amino-2-furyl)-2-propenoate were synthesized from the corresponding 4,5-dibromo derivatives, sodium azide and malononitrile. All compounds are characterized by UV spectral data; kinetics of nucleophilic substitution reactions with piperidine is presented, as well.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::5f0dc0e4f8021af34e98cdd0c5987b00 https://doi.org/10.1135/cccc19840984 Zobrazit plný text záznamu