1984
DOI: 10.1055/s-1984-30965
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Synthesis of Heterocyclic Compounds; XL. Regioselective Synthesis of 4-Substituted 2-Amino-5-cyano-6-methoxy-3-benzenesulfonylpyridines

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Cited by 6 publications
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“…Thus, compound 1 reacts under TEA catalysis with α,β-unsaturated nitriles (2a,b) in refluxing ethanol to afford 2-amino-3-phenylsulfonyl-4-aryl-5-carbonitrile pyridines 3a,b as coloured solid products [11]. The IR spectrum of these products showed in each case, absorption bands at ν 3350-3400, 2220, and 1610 cm -1 corresponding to NH 2 , CN, and C=N groups respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Thus, compound 1 reacts under TEA catalysis with α,β-unsaturated nitriles (2a,b) in refluxing ethanol to afford 2-amino-3-phenylsulfonyl-4-aryl-5-carbonitrile pyridines 3a,b as coloured solid products [11]. The IR spectrum of these products showed in each case, absorption bands at ν 3350-3400, 2220, and 1610 cm -1 corresponding to NH 2 , CN, and C=N groups respectively.…”
Section: Resultsmentioning
confidence: 99%