عنوان المقالة:Synthesis and Characterization of New Schiff Bases Heterocyclic Compounds and Their N-Acyl, Thiourea and Imidazole Derived from D-Erythroascorbic Acid Synthesis and Characterization of New Schiff Bases Heterocyclic Compounds and Their N-Acyl, Thiourea and Imidazole Derived from D-Erythroascorbic Acid
Muna S. Al-Rawi, Jumbad H. Tomma, Abdul-Jabber A. Mukhlus, Ammar H. Al-Dujaili*
المؤلفون بالإنجليزي
Muna S. Al-Rawi, Jumbad H. Tomma, Abdul-Jabber A. Mukhlus, Ammar H. Al-Dujaili*
الملخص العربي
The new Schiff bases derived from D-erythroascorbic acid containing heterocyclic unit were synthesized by condensation of D-erythroascorbic acid with aromatic amine (containing 1,3,4-oxadiazole or 1,3,4-thiadiazole unit) in dry benzene using glacial acetic acid as a catalyst. D-erythroascorbic acid[IV] was synthesized by four steps (Scheme 1), while the primary aromatic amine which is containing 1,3,4-oxadiazole[VII] or 1,3,4-thiadiazole[XII] synthesized by the reaction of 4-methoxybenzoyle- hydrazine[VI] with 4-aminobenzoic acid or by the reaction tuloic acid with thiosemicarbazide, respectively in the presence of POCl3. The new imidazole derivatives were synthesized by three-steps reactions starting with corresponding Schiff bases[VIII ] or[XIII ]. N-acyl compounds[IX]a,b and[XIV]a,b were synthesized by addition reaction of acid chloride to imine group of Schiff bases in dry benzene. The second step include reaction of thiourea with N-acyl derivatives in Na2CO3 medium to yield N-thiourea compounds[X]a,b and[XV]a,b. The third step involves cyclization reaction of N-thiourea derivatives with benzoin in DMF to result new imidazole derivatives[XI]a,b and[XVI]a,b.
الملخص الانجليزي
The new Schiff bases derived from D-erythroascorbic acid containing heterocyclic unit were synthesized by condensation of D-erythroascorbic acid with aromatic amine (containing 1,3,4-oxadiazole or 1,3,4-thiadiazole unit) in dry benzene using glacial acetic acid as a catalyst. D-erythroascorbic acid[IV] was synthesized by four steps (Scheme 1), while the primary aromatic amine which is containing 1,3,4-oxadiazole[VII] or 1,3,4-thiadiazole[XII] synthesized by the reaction of 4-methoxybenzoyle- hydrazine[VI] with 4-aminobenzoic acid or by the reaction tuloic acid with thiosemicarbazide, respectively in the presence of POCl3. The new imidazole derivatives were synthesized by three-steps reactions starting with corresponding Schiff bases[VIII ] or[XIII ]. N-acyl compounds[IX]a,b and[XIV]a,b were synthesized by addition reaction of acid chloride to imine group of Schiff bases in dry benzene. The second step include reaction of thiourea with N-acyl derivatives in Na2CO3 medium to yield N-thiourea compounds[X]a,b and[XV]a,b. The third step involves cyclization reaction of N-thiourea derivatives with benzoin in DMF to result new imidazole derivatives[XI]a,b and[XVI]a,b.