Literature DB >> 19650745

The role of sulfamide derivatives in medicinal chemistry: a patent review (2006-2008).

Allen B Reitz1, Garry R Smith, Michael H Parker.   

Abstract

BACKGROUND: The sulfamide (R(2)NSO(2)NR(2)) functionality is an acceptable functional group in medicinal chemistry when incorporated into putative small-molecule therapeutics, as it has the potential to form several electrostatic interactions with protein and other targets. The clinically-useful broad spectrum antibiotic doripenem contains a mono-substituted sulfamide. The sulfamide functional group is often found to substitute for sulfonamide, sulfamate or urea functionality. OBJECTIVE/
METHOD: During the period of 2006-2008, there were nine published patents in which all or most reported compounds contained the sulfamide functional group. There are also patents in which the structures disclosed contain a cyclic sulfamide functional group. Further, there are patents published during this timeframe that contain only a few sulfamide-containing examples, typically as a bioisosteric replacement for a sulfonamide moiety. In this review, we focus on those published patents in which most compounds disclosed are sulfamides and only briefly highlight examples in which sulfamides are included among a large list of other suitable functionalities.
CONCLUSION: While the sulfamide functionality is still fairly under-represented in medicinal chemistry, it is a valuable and versatile group that will gain increasing acceptance and favor in the future.

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Year:  2009        PMID: 19650745     DOI: 10.1517/13543770903185920

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  15 in total

1.  Complementary regioselectivity in the Cu(I)-catalyzed diamination of conjugated dienes to form cyclic sulfamides.

Authors:  Richard G Cornwall; Baoguo Zhao; Yian Shi
Journal:  Org Lett       Date:  2010-12-30       Impact factor: 6.005

2.  Chemoselective amination of propargylic C(sp³)-H bonds by cobalt(II)-based metalloradical catalysis.

Authors:  Hongjian Lu; Chaoqun Li; Huiling Jiang; Christopher L Lizardi; X Peter Zhang
Journal:  Angew Chem Int Ed Engl       Date:  2014-05-19       Impact factor: 15.336

3.  Synthesis, anti-cancer screening and tyrosyl-DNA phosphodiesterase 1 (Tdp1) inhibition activity of novel piperidinyl sulfamides.

Authors:  Jung Ho Jun; Vineet Kumar; Thomas S Dexheimer; Iwona Wedlich; Marc C Nicklaus; Yves Pommier; Sanjay V Malhotra
Journal:  Eur J Pharm Sci       Date:  2017-10-13       Impact factor: 4.384

4.  Potent inhibition of Norwalk virus by cyclic sulfamide derivatives.

Authors:  Dengfeng Dou; Kok-Chuan Tiew; Guijia He; Sivakoteswara Rao Mandadapu; Sridhar Aravapalli; Kevin R Alliston; Yunjeong Kim; Kyeong-Ok Chang; William C Groutas
Journal:  Bioorg Med Chem       Date:  2011-08-27       Impact factor: 3.641

5.  Stereoselective radical amination of electron-deficient C(sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination.

Authors:  Hongjian Lu; Yang Hu; Huiling Jiang; Lukasz Wojtas; X Peter Zhang
Journal:  Org Lett       Date:  2012-09-21       Impact factor: 6.005

6.  Photochemically Mediated Nickel-Catalyzed Synthesis of N-(Hetero)aryl Sulfamides.

Authors:  R Thomas Simons; Georgia E Scott; Anastasia Gant Kanegusuku; Jennifer L Roizen
Journal:  J Org Chem       Date:  2020-05-04       Impact factor: 4.354

7.  Asymmetric Palladium-Catalyzed Alkene Carboamination Reactions for the Synthesis of Cyclic Sulfamides.

Authors:  Zachary J Garlets; Kaia R Parenti; John P Wolfe
Journal:  Chemistry       Date:  2016-03-10       Impact factor: 5.236

8.  Development of Tetramethylenedisulfotetramine (TETS) Hapten Library: Synthesis, Electrophysiological Studies, and Immune Response in Rabbits.

Authors:  Bogdan Barnych; Natalia Vasylieva; Tom Joseph; Susan Hulsizer; Hai M Nguyen; Tomas Cajka; Isaac Pessah; Heike Wulff; Shirley J Gee; Bruce D Hammock
Journal:  Chemistry       Date:  2017-05-30       Impact factor: 5.236

9.  Influence of catalyst structure and reaction conditions on anti- versus syn-aminopalladation pathways in Pd-catalyzed alkene carboamination reactions of N-allylsulfamides.

Authors:  Ryan M Fornwald; Jonathan A Fritz; John P Wolfe
Journal:  Chemistry       Date:  2014-06-17       Impact factor: 5.236

10.  Synthesis of unsymmetrical sulfamides and polysulfamides via SuFEx click chemistry.

Authors:  Ryan W Kulow; Jiun Wei Wu; Cheoljae Kim; Quentin Michaudel
Journal:  Chem Sci       Date:  2020-07-13       Impact factor: 9.825

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