Studies on Azaindolizine Compounds. XIV. Transetherification in s-Triazolo [1,5-a] pyrimidines.
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概要
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Ten kinds of alkoxy-s-triazolo [1,5-a] pyrimidines were synthesized by reaction of the corresponding chloro derivatives with sodium alkoxides and the transetherification reaction of these compounds was investigated. It was clear that the alkoxyl group at 7-position was transetherified more easily than that at 5-position in s-triazolo [1,5-a]-pyrimidines.
- 公益社団法人日本薬学会の論文
- 1963-07-25
著者
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