REACTION OF 3-PYRIDINE WITH SUBSTITUTED ACETOPHENONES

DOI: 10.1007/BF00472388

Source and publish data:

Chemistry of Heterocyclic Compounds p. 292 - 296 (1989)

Update date:2022-08-05

Topics:

Authors:

Kozlov, N.S.

Mikhalevskaya, S.V.

Serzhanina, V.A.

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Article abstract of DOI:10.1007/BF00472388

The reaction of 3-pyridine with substituted acetophenones in the presence of a proton catalyst leads to 1-aryl-3-(3-pyridyl)benzoquinolines.Noncyclic amino ketones - <1-aryl-3-(3-pyridyl)-3-(2-naphthylamino)>-1-propanones - precede the formation of the cyclic products.The IR, UV, PMR, and mass spectra of the synthesized compounds are discussed.

Full text of DOI:10.1007/BF00472388

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Product name:<1-(4-methylphenyl)-3-(3-pyridyl)-3-(2-naphthylamino)>-1-propanone

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