Literature DB >> 28567464

A facile synthesis of sulfonylureas via water assisted preparation of carbamates.

Dinesh Kumar Tanwar1, Anjali Ratan, Manjinder Singh Gill.   

Abstract

A novel and simple approach to the synthesis of sulfonylureas has been reported. It involved the reaction of various amines with diphenyl carbonate to yield the corresponding carbamates, which subsequently reacted with different sulphonamides to produce different sulfonylureas in excellent yields. The first reaction of diphenyl carbonate with amines was carried out in aqueous : organic (H2O : THF, 90 : 10) medium at room temperature to produce carbamates that paved a straightforward route to sulfonylureas after reaction with sulfonamides. The above process avoided traditional multistep protocols and the use of hazardous, irritant, toxic and moisture sensitive reagents such as phosgene, isocyanates and/or chloroformates.

Entities:  

Year:  2017        PMID: 28567464     DOI: 10.1039/c7ob00872d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

1.  Crystal structure of 4-bromo-N-(propyl-carbamo-yl)benzene-sulfonamide.

Authors:  Mustafa Bookwala; Saloni Patel; Patrick T Flaherty; Peter L D Wildfong
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2022-04-07

2.  Protonation and anion-binding properties of aromatic sulfonylurea derivatives.

Authors:  D Barišić; N Cindro; N Vidović; N Bregović; V Tomišić
Journal:  RSC Adv       Date:  2021-07-07       Impact factor: 4.036

Review 3.  Selective small-molecule EPAC activators.

Authors:  Urszula Luchowska-Stańska; David Morgan; Stephen J Yarwood; Graeme Barker
Journal:  Biochem Soc Trans       Date:  2019-10-31       Impact factor: 5.407

  3 in total

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