2013European Chemical BulletinOpen access

SYNTHESIS OF UNSYMMETRICAL THIOUREA DERIVATIVES

Asieh Yahyazadeh, Zahra Ghasemi

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Abstract

A series of thiourea derivatives have been synthesized. Thiourea derivatives show a broad spectrum of biological activities such as antibacterial, antiviral, anticancer, anticonvulsion, analgesic an HDL-elevating. Ethyl isothiocyanate and aromatic amines were mixed and stirred at room temperature in acetone for 15h to give the corresponding thioureas in high yields. Their structures were confirmed by IR and 1H-NMR. By addition e-donor groups to aromatic amines, thioureas were synthesized in high yields.

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A series of thiourea derivatives have been synthesized. Thiourea derivatives show a broad spectrum of biological activities such as antibacterial, antiviral, anticancer, anticonvulsion, analgesic an HDL-elevating. Ethyl isothiocyanate and aromatic amines were mixed and stirred at room temperature in acetone for 15h to give the corresponding thioureas in high yields. Their structures were confirmed by IR and 1H-NMR. By addition e-donor groups to aromatic amines, thioureas were synthesized in high yields.

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Available abstract

A series of thiourea derivatives have been synthesized. Thiourea derivatives show a broad spectrum of biological activities such as antibacterial, antiviral, anticancer, anticonvulsion, analgesic an HDL-elevating. Ethyl isothiocyanate and aromatic amines were mixed and stirred at room temperature in acetone for 15h to give the corresponding thioureas in high yields. Their structures were confirmed by IR and 1H-NMR. By addition e-donor groups to aromatic amines, thioureas were synthesized in high yields.

Key concepts: Thiourea, Isothiocyanate, Chemistry, Acetone, Broad spectrum, Organic chemistry, Phenyl isothiocyanate, Combinatorial chemistry

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