Extended knowledge of 159326-69-9

There is still a lot of research devoted to this compound(SMILES:O=C(C1=CC=CN1N)N)Application In Synthesis of 1-Aminopyrrole-2-carboxamide, and with the development of science, more effects of this compound(159326-69-9) can be discovered.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Synthesis of pyrrolo[2,1-f][1,2,4]triazine congeners of nucleic acid purines via the N-amination of 2-substituted pyrroles, published in 1994-08-31, which mentions a compound: 159326-69-9, Name is 1-Aminopyrrole-2-carboxamide, Molecular C5H7N3O, Application In Synthesis of 1-Aminopyrrole-2-carboxamide.

The synthesis of several new 4-mono- and 2,4-disubstituted pyrrolo[2,1-f][1,2,4]triazines is described. Key intermediates 1-aminopyrrole-2-carbonitrile (3) and 1-amino-5-ethylpyrrole-2-carbonitrile (15) were obtained by N-amination of the corresponding pyrrole-2-carboxaldehyde followed by CHO → CN conversion with either hydroxylamine-O-sulfonic acid for 3 or O-mesitylenesulfonylhydroxylamine for 15. Cyclization of 3 or 15 with a variety of amidine reagents or, after conversion of 3 to its corresponding amide, base-catalyzed annulation completed the synthesis of the title products.

There is still a lot of research devoted to this compound(SMILES:O=C(C1=CC=CN1N)N)Application In Synthesis of 1-Aminopyrrole-2-carboxamide, and with the development of science, more effects of this compound(159326-69-9) can be discovered.

Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica