Suhair Mansour Jambi
University of Jedahh, Saudi Arabia
Title: Synthesis and characterization of N-eth–N`(4`- methylthiazol) -2ylthiourea
Biography
Biography: Suhair Mansour Jambi
Abstract
Thiourea and its derivatives have long been attracting considerable attention due to their biological importance. The facile synthesis of thioureas enabled the preparation of their numerous derivatives, most of which have been evaluated for their biological activities for example herbicidal, insecticidal, antiviral, antifungal, antibacterial. The compound was prepared by boiling under reflux an equal molar ratio of 2-methyl-4-methylthiazole and ethylisothiocyanate for 10 hrs in ethanol as solvent. The reaction product was filtered off, yellow crystals washed with ethanol and recrystallized with ethanol. Yield: 80%; m.p: 233 ÌŠC. Anal. Calc. for C7H11N3S2 (201 g mol-1): C, 41.73; H, 4.97; N, 20.86; S, 31.79 Found: C,42.12; H, 5.05; N, 20.61; S, 31.38. The main IR spectral bands, useful for suggesting the bonding sites of 1- (4-methylthiazol-2-yl)-3 –ethyl thiourea are present. The infrared spectrum of compound, measured in a KBr disc, shows two band at 3435 and 3177 cm-1, assignable to (N1H) and (N2H) respectively, the band at 823 (C=S), 1476.00 (CH3), 680 (C-S-C), 1577; 1535; 1506 C (Tz ring). 1H-NMR â–¡= 1.16 ppm (CH3), â–¡= 2.53 ppm (CH2), â–¡= 2.23 ppm (CH3), â–¡= 6.61 ppm (H-5), â–¡= 9.66 ppm (N2H), â–¡= 11.48 ppm (N1H). 13C-NMR: â–¡= 14.30; 48.20 ppm (ethyl carbons), â–¡= 106.40; 145.90; 161.80 ppm (thiazol carbons), â–¡= 178.50 ppm (C=S), â–¡= 17.00 ppm (CH3). The spectrum of 1- (4-methylthiazol-2-yl)-3 –ethyl thiourea shows a peak at m/z 201 corresponding to a molecular weight of the compound. The molecular compound A loses H2S forming B, loses EtNH2 forming C, loses EtSCN forming D and E.