Synthesis of Pyridazin-3(2H)-one Derivatives by the Reaction of CH-Acids with Dichlorodiazadienes

The reactions of 4,4-dichloro-1,2-diazabuta-1,3-dienes with dimethyl malonate, cyanoacetic esters and ethyl acetoacetate provided straightforward access to highly functionalized pyridazine derivatives. The approach was found to be very general for the highly efficient synthesis of various pyridazine derivatives which can be isolated in moderate to excellent yields. The possibility of their subsequent functionalization was demonstrated. Moreover, the absorption characteristics in the UV/Vis-range and luminescence were studied for all synthesized compounds. © 2020 Wiley-VCH GmbH

Authors
Sergeev P.G.1 , Khrustalev V.N. 2, 3 , Nenajdenko V.G. 1
Number of issue
38
Language
English
Pages
6085-6093
Status
Published
Volume
2020
Year
2020
Organizations
  • 1 Department of Chemistry, Lomonosov Moscow State University, Moscow, 119899, Russian Federation
  • 2 Peoples' Friendship University of Russia, Moscow, 117198, Russian Federation
  • 3 N. D. Zelinsky Institute of Organic Chemistry of RAS, 47 Leninsky Prospect, Moscow, 119991, Russian Federation
Keywords
Heterodienes; Nitrogen heterocycles; Nucleophilic substitution; Pyridazines; Spectral data
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