Catalyst-Free, Three-Component Synthesis of Amidinomaleimides

被引:1
|
作者
Swift-Ramirez, Wyatt R. [1 ]
Whalen, Lindsay A. [1 ]
Thompson, Lia K. [1 ]
Shoemaker, Kaylee E. [1 ]
Rubio, Aris R. [1 ]
Weiss, Gregory A. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Pharmaceut Sci, Irvine, CA 92697 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 18期
关键词
NEXT-GENERATION MALEIMIDE; N-SULFONYL AMIDINES; DERIVATIVES; TOXICITY; PRODUCTS; ENAMINES; AMINES; POTENT; AZIDE; AMIDE;
D O I
10.1021/acs.joc.4c01485
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Maleimide and amidine functionalities often appear in medicinal and natural product targets. We describe a catalyst-free, three-component coupling reaction for the synthesis of amidinomaleimides. This one-pot reaction fuses a broad range of secondary amines and aldehydes with azidomaleimides. The conditions are mild, simple, modular, high yielding, and amenable to aqueous solvents. Most reaction products can be sufficiently purified without column chromatography. The synthesis creates complex, multifunctional molecules with four different molecules, including a tripeptide, arrayed around an amidinomaleimide core.
引用
收藏
页码:13756 / 13761
页数:6
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