Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Tetrahedron Letters called A facile synthesis of meta- and para-terphenylglyoxamide-based peptidomimetics, Author is Yu, Tsz Tin; Bhadbhade, Mohan; Kuppusamy, Rajesh; Black, David St. C.; Kumar, Naresh, which mentions a compound: 7524-52-9, SMILESS is N[C@@H](CC1=CNC2=CC=CC=C12)C(OC)=O.[H]Cl, Molecular C12H15ClN2O2, Electric Literature of C12H15ClN2O2.
A series of meta- and para-terphenylglyoxamide peptidomimetics have been synthesized by the ring-opening of 5-(biphenylyl)-N-acylisatins with alcs., amines and amino acid Me esters. The starting 5-(biphenylyl)isatins were synthesized via the Suzuki-Miyaura coupling reaction in a convenient and efficient manner.
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Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem