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- W2951143948 abstract "Abstract magnified image Reaction of 2‐methylthio‐4(3 H )‐quinazolinone with chloroacetone, ω‐bromoacetophenone or ethyl bromoacetate in different solvents (methanol, acetonitrile, dimethylformamide and toluene) using sodium methoxide or potassium carbonate as a base were studied. Regioselective N (3) ‐alkylation took place in toluene using potassium carbonate, whereas in dimethylformamide O‐acylmethyl derivatives were obtained. However chloroacetone reacted with 2‐methylthio‐4(3 H )‐quinazolinone under various conditions to give a mixture of N (3) /O‐isomers." @default.
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- W2951143948 date "2008-03-01" @default.
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- W2951143948 title "Regioselective synthesis of N<sub>(3)</sub>‐ and O‐acylmethyl derivatives of 2‐methylthio‐4(3<i>H</i>)‐quinazolinone" @default.
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- W2951143948 doi "https://doi.org/10.1002/jhet.5570450250" @default.
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