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Sinteza i biološka evaluacija nekih pirimidina, pirimido2,1-b1,3tiazina i tiazolo3,2-apirimidin derivata

机译:某些嘧啶,嘧啶2,1-b 1,3噻嗪和噻唑洛3,2-a嘧啶衍生物的合成及生物学评价

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摘要

4,6-Diamino-1H-pyrimidine-2-thione (1) was used for the preparation of the pyrimidine derivatives 2-5. Compound 5 was cyclized to produce pyrimido[2,1-b][1,3]thiazine derivatives 6, which was condensed with p-chlorobenzaldehyde to give compound 7. The latter compound was reacted with hydroxylamine to give isoxazolo[4,5-d]thiazino[2,3-a]pyrimidines 8. Compound 8b was treated with 2-chloroethyl methyl ether to afford compound 9. Similarly, compound 3 was reacted with chloroacetic acid to give thiazolo[3,2-a]pyrimidine 10, which was condensed with p-chlorobenzaldehyde to give compound 11. Compound 11 was condensed with hydroxylamine to give isoxazolo[4,5-d]thiazolo[2,3-a]pyrimidine 12. Compound 12b was treated with 2-chloroethyl methyl ether to afford compound 13. The biological evaluation of some prepared products showed that many of them revealed promising antimicrobial activity.
机译:使用4,6-二氨基-1H-嘧啶-2-硫酮(1)制备嘧啶衍生物2-5。将化合物5环化以产生嘧啶并[2,1-b] [1,3]噻嗪衍生物6,将其与对氯苯甲醛缩合得到化合物7。使后者与羟胺反应得到异恶唑并[4,5-]。 d] thiazino [2,3-a] pyrimidines 8.将化合物8b用2-氯乙基甲基醚处理,得到化合物9。类似地,化合物3与氯乙酸反应,得到thiazolo [3,2-a] pyrimidine 10,将其与对氯苯甲醛缩合得到化合物11。将化合物11与羟胺缩合得到异恶唑并[4,5-d]噻唑并[2,3-a]嘧啶12。将化合物12b用2-氯乙基甲基醚处理至得自化合物13。对某些制备产品的生物学评估表明,其中许多产品显示出有希望的抗菌活性。

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