FORMATION OF A DERIVATIVE OF 3,3,5-TRICARBONYL-1,2,3,4-TETRAHYDROPYRIDINE UNDER THE CONDITIONS OF THE HANTZSCH SYNTHESIS

DOI: 10.1007/BF00542780

Source and publish data:

Chemistry of Heterocyclic Compounds p. 410 - 414 (1986)

Update date:2022-08-03

Topics: Derivative Formation Experimental conditions Hantzsch synthesis

Authors:

Chekavichus, B.S.

Sausin, A.E.

Zolotoyabko, R.M.

Liepin'sh, E.E.

Mazheika, I.B.

Dubur, G.Ya.

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Article abstract of DOI:10.1007/BF00542780

An ester of p-nitrobenzoylacetic acid is cyclized under the action of hexamethylentetramine and ammonium acetate to 3,5-diethoxycarbonyl-3-p-nitrobenzoyl-6-p-nitrophenyl-1,2,3,4-tetra-hydropyridine, the structure of which has been established by NMR, UV,

Full text of DOI:10.1007/BF00542780

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Product name:3,5-diethoxycarbonyl-3-(p-nitrobenzoyl)-6-(p-nitrophenyl)-1,2,3,4-tetrahydropyridine

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