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新产品编号:2409895

Chemical Name: 3-(3-Quinolinyl)-3-[1-[3-(1,4,5,6-tetrahydropyrimidin-2-ylamino)benzoyl]piperidin-4-ylcarboxamido]propionic acid
项目整合开发状态: Biological Testing
项目研究机构: Johnson & Johnson (Originator)
合成路线:The title compound is obtained by solid-phase synthesis using a 2-chlorotrityl chloride resin: Attachment of N-Fmoc-3-amino-3-(3-quinolinyl)propionic acid (I) to the chlorotrityl resin provides the protected amino acid-bound resin (II).Removal of the N-Fmoc group of (II) is achieved by treatment with piperidine in DMF to yield (III).Acylation of amine (III) with N-Fmoc-isonipecotic acid (IV) employing HATU furnishes amide (V).After Fmoc group deprotection in (V) with piperidine,the resultant amine resin (VI) is coupled to the guanidino acid (VII),producing resin (VIII).The title compound is finally cleaved from the resin by treatment with trifluoroacetic acid.
📌 参考资料/链接:
参考文献标题:Synthesis and biological evaluation of potent isonipecotamide-based vitronectin receptor antagonists
文献作者:Ghosh,S.; et al.
参考来源:224th ACS Natl Meet (Aug 18 2002,Boston) 2002,Abst MEDI 94