A facile synthesis of [14C]pyrithiobac‐sodium |
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Abstract: | Condensation of thiourea 1 with diethyl malonate 2 in the presence of sodium methoxide furnished 4,6‐dihydroxy‐2‐mercaptopyrimidine 3 . Compound 3 on methylation with diazomethane followed by oxidation with H5IO6/CrO3 in ethyl acetate gave 4,6‐dimethoxy‐2‐methylsulphonylpyrimidine 5 . Compound 5 on condensation with 2‐mercapto‐6‐chlorobenzoic acid in the presence of a phase transfer catalyst, tetrabutylammonium bromide and sodium carbonate gave the title compound – pyrithiobac‐sodium 6 with an overall yield of > 35% starting from thiourea. Following the above standardized procedure, using [14C]‐thiourea in lieu of thiourea, 14C labelled product 6 , was synthesized with an overall radiochemical yield > 30% (with respect to [14C]‐thiourea) for further evaluations of environmental fate of 6 , in soils and plants. Copyright © 2006 John Wiley & Sons, Ltd. |
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Keywords: | [14C]‐Thiourea 4,6‐dihydroxy‐2‐mercaptopyrimidine 4,6‐dimethoxy‐2‐methylsulphonyl‐pyrimidine [14C]‐pyrithiobac‐sodium [14C]sodium 2‐chloro‐6‐(4,6‐dimethoxy‐2‐pyrimidinylthio)benzoate |
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