Synthesis and Evaluation of New 6-formyl-oxazolo[3,2-a]pyrimidine derivatives as Potential Src Kinase Inhibitors

J. Guillon, François Hallé, Solène Savrimoutou, S. Moreau, D. Caignard, P. Sonnet
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Abstract

The tyrosine-protein kinase Src, also known as proto-oncogene c-Src or simply c-Src, is a non-receptor tyrosine kinase protein that has been shown to be involved in the regulation of important cellular processes including migration, survival and proliferation. In fact, Src activation has been associated with multiple cancers, such as colon, breast, pancreas, lung, or brain (Roskoski, R. Jr. Pharmacol. Res. 2015, 94, 9-25; Creedon, H., et al., Crit. Rev. Oncog. 2012, 17, 145-159). There are only few Src inhibitors in clinical development, therefore, there is an urgent need to identify new low molecular weight therapeutics able to inhibit Src and, thus, to modulate aberrant pathways leading to malignant transformation of cells (Lu, X.L., et al., Curr. Med. Chem. 2012, 19, 1821-1829). Heterocyclic compounds attracted a lot of attention because of their wide spread biological activities. Thus, we have previously reported the synthesis of biological active heterocyclic derivatives based on the reactivity of the amidine moiety of 2-amino-2-oxazolines 2 with bis-electrophiles (Massip, S., et al., Bioorg. Med. Chem. 2006, 14, 2697-2719). https://ibb.co/hzkMnJ In a preliminary screening testing our heterocycles library, we have identified a “hit” (compound 1d) derived from various substituted 6-formyl-oxazolo[3,2-a]pyrimidines as a new Src kinase inhibitor (IC50 = 4 µM). These original oxazolo[3,2-a]pyrimidine derivatives 1a-k were synthesized through a Diels-Alder cycloaddition of alkylidene derivatives of 2-amino-2-oxazoline (compounds 3a-k) with acrolein, as an electron-poor dienophile, a reaction previously described by our group (Guillon, J., et al., Synlett 2002, 8, 1249-1252). Versatility given by this reaction allowed us to access a promising family of diversely substituted 6-formyl-oxazolo[3,2-a]pyrimidines with inhibitory effect on Src kinase. Acknowledgments: This work was supported by a grant from Ligue Contre le Cancer (Gironde, Bordeaux, France).
新型6-甲酰基恶唑[3,2-a]嘧啶衍生物作为Src激酶抑制剂的合成与评价
酪氨酸蛋白激酶Src,也被称为原癌基因c-Src或简称c-Src,是一种非受体酪氨酸激酶蛋白,已被证明参与重要细胞过程的调节,包括迁移、存活和增殖。事实上,Src活化与多种癌症有关,如结肠癌、乳腺癌、胰腺癌、肺癌或脑癌(Roskoski, R. Jr. Pharmacol)。Res. 2015, 94, 9-25;克里登,H.等人,克里特。农业学报,2012,17(1):145-159。临床开发中的Src抑制剂很少,因此,迫切需要找到新的低分子量疗法,能够抑制Src,从而调节导致细胞恶性转化的异常途径(Lu, X.L等,Curr。医学化学,2012,19,1821-1829)。杂环化合物因其广泛的生物活性而备受关注。因此,我们之前已经报道了基于2-氨基-2-恶唑啉2的脒部分与双亲电试剂的反应性合成具有生物活性的杂环衍生物(Massip, S.等人,Bioorg.)。医学化学,2006,14,2697-2719)。https://ibb.co/hzkMnJ在我们的杂环文库的初步筛选测试中,我们已经确定了一个“hit”(化合物1d),它来源于各种取代的6-甲酰基恶唑[3,2-a]嘧啶,作为一种新的Src激酶抑制剂(IC50 = 4µM)。这些原始的恶唑[3,2-a]嘧啶衍生物1a-k是通过2-氨基-2-恶唑啉的烷基基衍生物(化合物3a-k)与丙烯醛的Diels-Alder环加成合成的,丙烯醛是一种电子贫的亲二酚,该反应之前被我们的团队描述过(Guillon, J., et al., Synlett 2002, 8, 1249-1252)。该反应的多功能性使我们能够获得具有抑制Src激酶作用的不同取代的6-甲酰基恶唑[3,2-a]嘧啶家族。致谢:这项工作得到了法国癌症协会(法国波尔多吉伦特)的资助。
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