Abstract
A study of the reaction of quinazoline derivatives with acid chlorides in the absence of acids has shown that alkyl 2-(4,4-diphenyl-1,2,3,4-tetrahydro-2-quinazolinylidene)acetates undergo C-acylation. The molecular structure of methyl 2-(4,4-diphenyl-1,2,3,4-tetrahydro-2-quinazolinylidene)-3-oxobutanoate has been investigated by X-ray analysis.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 886–983, June, 2007.
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Gromachevskaya, E.V., Kaigorodova, E.A., Zavodnik, V.E. et al. Studies on quinazoline chemistry. 4. Unexpected route of acylation of alkyl 2-(4,4-diphenyl-1,2,3,4-tetrahydro-2-quinazolinylidene)acetates. Molecular structure of methyl 2-(4,4-diphenyl)-1,2,3,4-tetrahydro-2-quinazolinylidene)-3-oxobutanoate. Chem Heterocycl Compd 43, 748–754 (2007). https://doi.org/10.1007/s10593-007-0121-y
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DOI: https://doi.org/10.1007/s10593-007-0121-y