1986
DOI: 10.1002/jhet.5570230205
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Synthesis of 6‐arylazo‐substituted 5‐hydroxy‐2‐hydroxymethyl‐4‐pyridones and related compounds

Abstract: 5‐Hydroxy‐2‐hydroxymethyl‐4‐pyridone (1) and 5‐hydroxy‐2‐hydroxymethyl‐1‐methyl‐4‐pyridone (2) reacted with arenediazonium salts to give 6‐arylazo‐substituted compounds 3a‐d and 4a‐d, respectively. Compounds 3a‐d were methylated with diazomethane to afford 6‐arylazo‐2‐hydroxymethyl‐4,5‐dimethoxypyridines 5a‐d.

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Cited by 2 publications
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“…Treatment of KA with thionyl chloride in DMF at room temperature, followed by reaction with potassium salts of benzoic acids in DMF at [110][111][112][113][114][115][116][117][118][119][120] • C, gave benzoate derivatives 269 in good yields.…”
Section: Scheme 81mentioning
confidence: 99%
“…Treatment of KA with thionyl chloride in DMF at room temperature, followed by reaction with potassium salts of benzoic acids in DMF at [110][111][112][113][114][115][116][117][118][119][120] • C, gave benzoate derivatives 269 in good yields.…”
Section: Scheme 81mentioning
confidence: 99%