Bridged Bicyclic gamma-Sultams by Intramolecular Flow Photochemical [2+2] Cycloaddition

13 September 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

An elegant synthetic approach to the construction of a novel saturated heterocycle – 2-thia-3-azabicyclo[2.1.1]hexane 2,2-dioxide – was designed. The key step included intramolecular flow photochemical [2 + 2] cycloaddition of appropriately substituted dienes, in turn obtained from readily available starting materials on a multigram scale. Further synthetic transformations of the resulting bicyclic compounds enabled the preparation of numerous functionalized derivatives useful for early drug discovery programs as promising isosteres of pyrrolidine, pyrrolidone, and gamma-sultams, and also demonstrated tolerance of the title bicyclic system towards typical organic chemistry reaction conditions.

Keywords

cycloaddition
sulfonamide
isostere
organosulfur compounds
photochemistry

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