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作 者:Davood Nematollahi Saied Saeed Hosseiny Davarani Pari Mirahmadpour Fahimeh Varmaghani
机构地区:[1]Faculty of Chemistry,Bu-Ali Sina University [2]Department of Chemistry,Faculty of Science,University of Shahid Beheshti [3]Department of Chemistry,Faculty of Science,Arak Branch,Islamic Azad University
出 处:《Chinese Chemical Letters》2014年第4期593-595,共3页中国化学快报(英文版)
基 金:Bu-Ali Sina University Research Council and Center of Excellence in Development of Environmentally Friendly Methods for Chemical Synthesis(CEDEFMCS) for their support of this work
摘 要:The electrochemical synthesis of some new sulfonamide derivatives was carried out via the electrochemical oxidation of 2,3-dihydrophthalazine-l,4-dione (1) in the presence of arylsulfinic acids (2a and 2b) as nucleophiles. The results show that, the electrogenerated phthalazine-l,4-dione (lox) participates in a Michael type addition reaction with 2a or 2b and via an EC mechanism to produce the corresponding sulfonamide derivatives. This method provides a one-pot procedure for the synthesis of new sulfonamide derivatives of potential biological significance in good yields without using toxic reagents at a carbon electrode in an environmentally friendly manner.The electrochemical synthesis of some new sulfonamide derivatives was carried out via the electrochemical oxidation of 2,3-dihydrophthalazine-l,4-dione (1) in the presence of arylsulfinic acids (2a and 2b) as nucleophiles. The results show that, the electrogenerated phthalazine-l,4-dione (lox) participates in a Michael type addition reaction with 2a or 2b and via an EC mechanism to produce the corresponding sulfonamide derivatives. This method provides a one-pot procedure for the synthesis of new sulfonamide derivatives of potential biological significance in good yields without using toxic reagents at a carbon electrode in an environmentally friendly manner.
关 键 词:2 3-Dihydrophthalazine- 1 4-dione Cyclic voltammetry Electrochemical synthesis Sulfonamide Arylsulfinic acid
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