1978
DOI: 10.1002/chin.197833241
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ChemInform Abstract: DERIVATIVES OF ARENESULFONIC ACIDS. IX. SYNTHESIS OF 4‐SULFAMIDO‐5‐(P‐ALKOXYBENZYL)PYRIMIDINES

Abstract: Das 5‐(p‐Alkoxybenzyl)‐4,6‐dichlorpyrimidin (I) wird mit dem doppelten Überschuß des Natriumsalzes von der Sulfamide (II) in Acetamid bei 100°C umgesetzt.

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“…Reaction of 4-propoxy-3-carbmethoxybenzylchloride [12] with malonic ester produced the substituted malonic ester, cyclization of which with guanidium hydrochloride into 2-aminopyrimidine III was carried out in the presence of sodium methoxide [13]. 2-Sulfonamidopyrimidine II was prepared by reacting 2-aminopyrimidine III and p-toluenesulfonylchloride in anhydrous pyridine.…”
mentioning
confidence: 99%
“…Reaction of 4-propoxy-3-carbmethoxybenzylchloride [12] with malonic ester produced the substituted malonic ester, cyclization of which with guanidium hydrochloride into 2-aminopyrimidine III was carried out in the presence of sodium methoxide [13]. 2-Sulfonamidopyrimidine II was prepared by reacting 2-aminopyrimidine III and p-toluenesulfonylchloride in anhydrous pyridine.…”
mentioning
confidence: 99%