A Noncatalytic Approach to Hetaryl‐Annulated 1,2,4‐Thiadiazine‐1,1‐dioxides

Abstract

A set of synthetic procedures was developed to yield functionalized pyrido‐, pyrimido‐, and thiazo‐annulated thiadiazine‐1,1‐dioxides on a preparative scale. In all cases the thiadiazine‐1,1‐dioxide ring closure was carried out through a reaction of hetaryl‐sulfonyl chlorides with amidines under mild noncatalytic conditions. In the case of 2‐chloropyridine‐3‐sulfonyl chloride derivatives and 2,4‐dichlorothiazole‐5‐sulfonyl chloride open‐chain sulfonylated amidine intermediates were isolated and then subjected to the cyclization step. The reaction with 2,4‐dichloropyrimidine‐5‐sulfonyl chloride gave rise to the corresponding thiadiazine‐1,1‐dioxides in one‐pot. Similarly, a reaction of 2‐chloropyridine‐3‐sulfonamide with lactime ethers proceeded in one‐pot readily giving the corresponding thiadiazine‐1,1‐dioxides. Remaining chlorine atoms on the prepared hetaryl‐annulated benzothiadiazine‐1,1‐dioxides readily undergo aromatic nucleophilic displacement reactions serving thus as additional variation points for the design of biologically potent compounds.

N,N-Dialkyl-N′-Chlorosulfonyl Chloroformamidines in Heterocyclic Synthesis. Part XII. Synthesis and Reactivity of the Pyrazolo[3,4-e][1,2,4]thiadiazine Ring System

“…[6,[11][12][13] The present derivatives of the pyrimido-thiadiazine ring system 13 were not stable in acidic media, such as chloroform without added stabiliser, which usually contains a small amount of HCl, or chromatography over silica gel and hence these products were purified over buffered silica and expeditiously characterised.…”