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, Article, Research Support, Non-U.S. Gov’t, Journal of the American Chemical Society called Benzoisothiazolone Organo/Copper-Cocatalyzed Redox Dehydrative Construction of Amides and Peptides from Carboxylic Acids using (EtO)3P as the Reductant and O2 in Air as the Terminal Oxidant, Author is Liebeskind, Lanny S.; Gangireddy, Pavankumar; Lindale, Matthew G., which mentions a compound: 180258-46-2, SMILESS is O=C(C1=NC(N)=CN1C)OCC.[H]Cl, Molecular C7H12ClN3O2, Electric Literature of C7H12ClN3O2.
Carboxylic acids and amine/amino acid reactants can be converted to amides and peptides at neutral pH within 5-36 h at 50° using catalytic quantities of a redox-active benzoisothiazolone and a copper complex. These catalytic “”oxidation-reduction condensation”” reactions are carried out open to dry air using O2 as the terminal oxidant and a slight excess of tri-Et phosphite as the reductant. Tri-Et phosphate is the easily removed byproduct. These simple-to-run catalytic reactions provide practical and economical procedures for the acylative construction of C-N bonds.
Although many compounds look similar to this compound(180258-46-2)Electric Literature of C7H12ClN3O2, numerous studies have shown that this compound(SMILES:O=C(C1=NC(N)=CN1C)OCC.[H]Cl), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com