Literature DB >> 16438524

A convenient preparation of heteroaryl sulfonamides and sulfonyl fluorides from heteroaryl thiols.

Stephen W Wright1, Kelly N Hallstrom.   

Abstract

Heteroaromatic thiols may be oxidized to the sulfonyl chloride at low temperature (-25 degrees C) by using 3.3 equiv of aqueous sodium hypochlorite. The reaction is rapid, avoids the use of chlorine gas, and succeeds with substrates that have previously been found to afford little or none of the sulfonamide product with other procedures. The method allows the preparation of the sulfonyl fluorides, which are stable enough to be purified and stored, making them potentially useful monomers in parallel chemistry efforts.

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Year:  2006        PMID: 16438524     DOI: 10.1021/jo052164+

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  10 in total

1.  Synthesis of aryl sulfonamides via palladium-catalyzed chlorosulfonylation of arylboronic acids.

Authors:  J Robb DeBergh; Nootaree Niljianskul; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2013-07-12       Impact factor: 15.419

2.  Iodine-catalyzed sulfonylation of sulfonyl hydrazides with tert-amines: a green and efficient protocol for the synthesis of sulfonamides.

Authors:  Jinyang Chen; Xiaoran Han; Lan Mei; Jinchuan Liu; Kui Du; Tuanwu Cao; Qiang Li
Journal:  RSC Adv       Date:  2019-10-02       Impact factor: 4.036

3.  N-Benzyl-pyridine-2-sulfonamide.

Authors:  Xiao-Ping Chen; Shou-Fa Han
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-05-29

4.  Design and in vitro activities of N-alkyl-N-[(8-R-2,2-dimethyl-2H-chromen-6-yl)methyl]heteroarylsulfonamides, novel, small-molecule hypoxia inducible factor-1 pathway inhibitors and anticancer agents.

Authors:  Jiyoung Mun; Adnan Abdul Jabbar; Narra Sarojini Devi; Shaoman Yin; Yingzhe Wang; Chalet Tan; Deborah Culver; James P Snyder; Erwin G Van Meir; Mark M Goodman
Journal:  J Med Chem       Date:  2012-07-24       Impact factor: 7.446

5.  Sulfonamide Synthesis via Calcium Triflimide Activation of Sulfonyl Fluorides.

Authors:  Paramita Mukherjee; Cristian P Woroch; Leah Cleary; Mark Rusznak; Ryan W Franzese; Matthew R Reese; Joseph W Tucker; John M Humphrey; Sarah M Etuk; Sabrina C Kwan; Christopher W Am Ende; Nicholas D Ball
Journal:  Org Lett       Date:  2018-06-11       Impact factor: 6.072

6.  Synthesis of Heteroaryl Sulfonamides from Organozinc Reagents and 2,4,6-Trichlorophenyl Chlorosulfate.

Authors:  James R Colombe; J Robb DeBergh; Stephen L Buchwald
Journal:  Org Lett       Date:  2015-06-11       Impact factor: 6.005

Review 7.  Direct synthesis of sulfenamides, sulfinamides, and sulfonamides from thiols and amines.

Authors:  Yan Cao; Shahrzad Abdolmohammadi; Roya Ahmadi; Alibek Issakhov; Abdol Ghaffar Ebadi; Esmail Vessally
Journal:  RSC Adv       Date:  2021-10-01       Impact factor: 4.036

8.  Facile one-pot synthesis of sulfonyl fluorides from sulfonates or sulfonic acids.

Authors:  Ying Jiang; Njud S Alharbi; Bing Sun; Hua-Li Qin
Journal:  RSC Adv       Date:  2019-05-07       Impact factor: 3.361

9.  Facile synthesis, crystal structure, biological evaluation, and molecular modeling studies of N-((4-acetyl phenyl) carbamothioyl) pivalamide as the multitarget-directed ligand.

Authors:  Aamer Saeed; Syeda Abida Ejaz; Aqsa Khalid; Pervaiz Ali Channar; Mubashir Aziz; Tanveer A Wani; Seema Zargar; Sidra Hassan; Hammad Ismail; Dania Khalid; Muhammad Zaffar Hashmi; Tuncer Hökelek; Abdullahi Tunde Aborode
Journal:  Front Chem       Date:  2022-09-26       Impact factor: 5.545

10.  Oxidative β-C-H sulfonylation of cyclic amines.

Authors:  R J Griffiths; W C Kong; S A Richards; G A Burley; M C Willis; E P A Talbot
Journal:  Chem Sci       Date:  2018-01-22       Impact factor: 9.825

  10 in total

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