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高效一锅法、三组分合成吡咯并[1,2-c]嘧啶衍生物库。

Efficient one-pot, three-component synthesis of a library of pyrrolo[1,2-c]pyrimidine derivatives.

机构信息

Research Center Oltchim, Ramnicu Valcea, Romania.

出版信息

ACS Comb Sci. 2012 Feb 13;14(2):101-7. doi: 10.1021/co2002125. Epub 2012 Feb 1.

Abstract

Herein is reported a simple and efficient one-pot three-component synthesis of pyrrolo[1,2-c]pyrimidine derivatives starting from various substituted pyrimidines, 2-bromoacetophenones, and electron deficient alkynes in epoxides acting both as reaction medium and HBr scavanger. This method proved to be very lucrative and avoids formation of ylide inactivation products. The synthesis represents an environmentally benign alternative to classical methods. The new library of compounds was briefly characterized regarding the improved Lipinski rule to asses the potential drug-likeness of the compounds. The majority of compounds are statisfing the Lipinski rule.

摘要

本文报道了一种简单高效的一锅法三组分合成吡咯并[1,2-c]嘧啶衍生物的方法,该方法以各种取代的嘧啶、2-溴苯乙酮和缺电子炔烃为原料,在环氧化合物中反应,环氧化合物既作为反应介质又作为 HBr 清除剂。该方法避免了叶立德失活产物的形成,证明非常有利。与经典方法相比,该合成代表了一种环境友好的替代方法。新化合物库的特点是简要描述了改进的 Lipinski 规则,以评估化合物的潜在药物相似性。大多数化合物符合 Lipinski 规则。

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