Abstract
3-Substituted 7-dialkylaminocoumarins were synthesized as a result of the photoreaction of 7-diethylaminocoumarin, 4-trifluoromethyl-7-diethylaminocoumarin, 4-chloro-7-diethylaminocoumarin, 4-(N-morpholino)-7-diethylaminocoumarin, and coumarin-102 (2,3,6,7-tetrahydro-9-methyl-1H,5H,11H-[1]-benzopyrano[6,7,8-ij]quinolizin-11-one) with iodobenzene, 3,4-dimethoxyiodobenzene, isopropyl iodide, and ethyl α-bromoacetate. It was established that electron-acceptor and electron-donor substituents in the 4 position accelerate photosubstitution. The spectral-luminescence characteristics of the compounds obtained were investigated.
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For Communication 5, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 1028–1032, August, 1990.
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Kirpichenok, M.A., Mel'nikova, L.M., Denisov, L.K. et al. Photochemical reactions of 7-aminocoumarins. 6. Reaction of 7-dialkylaminocoumarins with halo derivatives. Chem Heterocycl Compd 26, 858–862 (1990). https://doi.org/10.1007/BF00480856
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DOI: https://doi.org/10.1007/BF00480856