Synthesis of new Organic reagent by Vilsmeier – Haack reaction and estimation of pharmaceutical compounds (Mesalazine) containing aromatic amine groups

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Noor Al-Thakafy ◽  
Mohammed Al-Enizzi ◽  
Mohanad Saleh
2016 ◽  
Vol 23 (12) ◽  
Author(s):  
Tamara Marqués ◽  
Rodrigo Navarro ◽  
Alberto Gallardo ◽  
Carolina Garcia ◽  
Carlos Elvira ◽  
...  
Keyword(s):  

ChemPlusChem ◽  
2016 ◽  
Vol 82 (2) ◽  
pp. 315-322 ◽  
Author(s):  
Liang Han ◽  
Kaiqi Ye ◽  
Chenglong Li ◽  
Yuewei Zhang ◽  
Hongyu Zhang ◽  
...  

1979 ◽  
Vol 76 ◽  
pp. 381-382 ◽  
Author(s):  
Inmaculada Velasco ◽  
Santos Otín ◽  
Celso Gutiérrez-Losa

2019 ◽  
Author(s):  
Patrick Fier ◽  
Kevin M. Maloney

Herein we describe the development and application of a method for the mild, late-stage conversion of primary sulfonamides to several other other functional groups. These reactions occur via initial reductive deamination of sulfonamides to sulfinates via an NHC-catalyzed reaction of transiently formed <i>N</i>-sulfonylimines. The method described here is tolerant of nearly all common functional groups, as exemplified by the late-stage derivatization of several complex pharmaceutical compounds. Based on the prevalence of sulfonamide-containing drugs and building blocks, we have developed a method to enable sulfonamides to be applied as versatile synthetic handles for synthetic chemsitry.


2019 ◽  
Author(s):  
Patrick Fier ◽  
Kevin M. Maloney

Herein we describe the development and application of a method for the mild, late-stage conversion of primary sulfonamides to several other other functional groups. These reactions occur via initial reductive deamination of sulfonamides to sulfinates via an NHC-catalyzed reaction of transiently formed <i>N</i>-sulfonylimines. The method described here is tolerant of nearly all common functional groups, as exemplified by the late-stage derivatization of several complex pharmaceutical compounds. Based on the prevalence of sulfonamide-containing drugs and building blocks, we have developed a method to enable sulfonamides to be applied as versatile synthetic handles for synthetic chemsitry.


2019 ◽  
Author(s):  
Chem Int

Recycling is a crucial area of research in green polymer chemistry. Various developments in recycling are driven by Environmental concerns, interest in sustainability and desire to decrease the dependence on non-renewable petroleum based materials. Polyurethane foams [PUF] are widely used due to their light weight and superior heat insulation as well as good mechanical properties. As per survey carried Polyurethane Foam Association, 12 metric tonnes of polyurethane foam are discharged during manufacturing and/or processing and hence recycling of PUF is necessary for better economics and ecological reasons. In present study, rejects of PUF is subjected to reaction with a diethylene amine in presence of sodium hydroxide [NaOH] as catalyst, as a result depolymerised product containing hydroxyl and amine groups is obtained. Conventional and Microwave reaction for depolymerizing polyurethane foam have been carried, and best results are obtained by Microwave reaction. Further depolymerised product with hydroxyl and amine functionalities are reacted with bis (2-hydroxyethyl terephthalate) [BHET] obtained by recycling polyethylene terephthalate [PET] and sebacic acid, with stannous oxalate [FASCAT 2100 series] as catalyst to obtain Polyester amides. These Polyester amides having hydroxyl and amino groups in excess are cured with isocyanates-hexamethylene diisocyanate biuret [HDI biuret] and isophorone diisocyanate [IPDI] for coating applications. The coated films are characterized using physical, mechanical and chemical tests, which shows comparable physical, mechanical properties but alkali resistance is poor.


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