An unusual synthesis of 3-(2-(arylamino)thiazol-4-yl)-2H-chromen-2-ones from ethyl 2-(chloromethyl)-2-hydroxy-2H-chromene-3-carboxylate via benzopyran ring opening |
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Authors: | Kavitha Kotthireddy Srikrishna Devulapally Sridhar Balasubramanian Aparna Pasula |
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Institution: | 1.Department of Chemistry, College of Engineering, Jawaharlal Nehru Technological University, Hyderabad, Kukatpally, Hyderabad, Telangana, 500 085, India ;2.Center for X-Ray Crystallography, CSIR-Indian Institute of Chemical Technology, Hyderabad, Telangana, 500 007, India ; |
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Abstract: | An unusual and unexpected synthesis of 3-(2-(arylamino)thiazol-4-yl)-2H-chromen-2-ones has been observed by the reaction of ethyl 2-(chloromethyl)-2-hydroxy-2H-chromene-3-carboxylate with various arylthioureas in ethanol under mild reaction conditions with excellent yields. The ambiguity in the structure of the obtained products has been solved by recording its single-crystal X-ray analysis. This protocol has been found to be a novel approach for the preparation of title compounds via benzopyran ring opening. A systematic plausible mechanism has been proposed for the formation of the product. Also, an efficient one-pot three-component method has been demonstrated for the formation of title compounds starting from salicylaldehyde. |
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