A Concise Synthesis of N‐(1,3‐Thiazol‐2‐yl) Indoline‐5‐Sulfonic Acids and Sulfonyl Chlorides
摘要:
A general and practical synthetic method was developed for indoline-5-sulfonic acids hearing a thiazole heterocycle attached to the nitrogen atom. Two select sulfonic acids were further converted to their corresponding sulfonyl chlorides, key intermediates to the indoline-5-sulfonamide pharmacophore.
A Concise Synthesis of N‐(1,3‐Thiazol‐2‐yl) Indoline‐5‐Sulfonic Acids and Sulfonyl Chlorides
摘要:
A general and practical synthetic method was developed for indoline-5-sulfonic acids hearing a thiazole heterocycle attached to the nitrogen atom. Two select sulfonic acids were further converted to their corresponding sulfonyl chlorides, key intermediates to the indoline-5-sulfonamide pharmacophore.