Synthesis of New 1,3-Thiazolecarbaldehydes


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Abstract

H-Lithiation and Br-lithiation reactions of 1,3-thiazole were studied in order to obtain new thiazole derivatives. Four isomeric chloromethyl derivatives of 1,3-thiazole containing a protected aldehyde group like 2-(1,3-dioxolan-2-yl)-5-(chloromethyl)-1,3-thiazole, 5-(1,3-dioxolan-2-yl)-2-(chloromethyl)-1,3-thiazole, 4-(1,3-dioxolan-2-yl)-2-(chloromethyl)-1,3-thiazole, and 2-(1,3-dioxolan-2-yl)-4-(chloromethyl)-1,3-thiazole were synthesized. Their nucleophilic substitution reactions with dimethylamine and sodium methylthiolate were studied. New aldehydes of 1,3-thiazole series of low-molecular weight were obtained.

About the authors

V. O. Sinenko

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
Ukraine, ul. Murmanskaya 1, Kiev, 02094

S. R. Slivchuk

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
Ukraine, ul. Murmanskaya 1, Kiev, 02094

O. P. Mityukhin

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
Ukraine, ul. Murmanskaya 1, Kiev, 02094

V. S. Brovarets

Institute of Bioorganic Chemistry and Petrochemistry

Author for correspondence.
Email: brovarets@bpci.kiev.ua
Ukraine, ul. Murmanskaya 1, Kiev, 02094


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