Hys, Vasyl Y.; Milokhov, Demyd S.; Volovenko, Olesya B.; Konovalova, Irina S.; Shishkina, Svitlana V.; Volovenko, Yulian M. published the artcile< Synthetic Approach to Fused Azasultams with 1,2,4-Thiadiazepine Framework>, Synthetic Route of 112-63-0, the main research area is fused azasultam thiadiazepine preparation; azole pyrrole carboxylate sulfonamide heterocyclization.
Synthetic approach to fused azasultams with 1,2,4-thiadiazepine framework via base promoted protocols has been developed. 1H-Azole-2-carboxylates and N-(chloromethyl)-N-methylmethanesulfonamide were used as ambiphilic building blocks in the one-pot and two-step reaction sequences. Chem. behavior of the obtained azasultams in reactions with amines, hydrazine, DMFDMA, and NaBH4 was investigated. An enamino ketone derived from an azasultam was exploited in the synthesis of new pyrazole and pyrimidine heterocycles.
Synthesis published new progress about Condensation reaction (sulfa-Dieckmann). 112-63-0 belongs to class esters-buliding-blocks, and the molecular formula is C19H34O2, Synthetic Route of 112-63-0.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics