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Synthesis ofω-substituted 3-alkylorotic acids
Authors:A Ya Berlin  I A Korbukh
Institution:(1) Institute of Experimental and Clinical Oncology, Academy of Medical Sciences of the USSR, Moscow
Abstract:3-(ohgr-Phthalimidoalkyl)-5-carbethoxymethylenehydantoins were synthesized by the reaction ofohgr-phthalimidoalkylureas with ethyl oxalacetate and then converted to 3-(ohgr-aminoalkyl)orotic acids. Condensation of the latter with 6-chloropurine yielded 3-ohgr-(6-purinylamino)alkyljorotic acids.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 397–399, March, 1971.
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