scholarly journals Wasteful Azo Dyes as a Source of Biologically Active Building Blocks

Author(s):  
Ana Fernandes ◽  
Bruna Pinto ◽  
Lorenzo Bonardo ◽  
Beatriz Royo ◽  
M. Paula Robalo ◽  
...  

In this work, an environment-friendly enzymatic strategy was developed for the valorisation of dye-containing wastewaters. We set up biocatalytic processes for the conversion of azo dyes representative of the main classes used in the textile industry into valuable aromatic compounds: aromatic amines, phenoxazinones, phenazines, and naphthoquinones. First, purified preparations of PpAzoR azoreductase efficiently reduced mordant, acid, reactive, and direct azo dyes into aromatic amines, and CotA-laccase oxidised these compounds into phenazines, phenoxazinones, and naphthoquinones. Second, whole cells containing the overproduced enzymes were utilised in the two-step enzymatic conversion of the model mordant black 9 dye into sodium 2-amino-3-oxo-3H-phenoxazine-8-sulphonate, allowing to overcome the drawbacks associated with the use of expensive purified enzymes, co-factors, or exquisite reaction conditions. Third, cells immobilised in sodium alginate allowed recycling the biocatalysts and achieving very good to excellent final phenoxazine product yields (up to 80%) in water and with less impurities in the final reaction mixtures. Finally, one-pot systems using recycled immobilised cells co-producing both enzymes resulted in the highest phenoxazinone yields (90%) through the sequential use of static and stirring conditions, controlling the oxygenation of reaction mixtures and the successive activity of azoreductase (anaerobic) and laccase (aerobic).

2020 ◽  
Vol 17 ◽  
Author(s):  
Sultanat ◽  
Anam Ansari ◽  
Mohd Qamar ◽  
Shafiullah ◽  
Sartaj Tabassum ◽  
...  

Background: Corticosteroids are important group of polycyclic compounds having a wide range of pharmacological and physiological properties. Thiopyran derivatives are important building blocks of many biologically active compounds. Objective: Keeping in mind the wide range of application of corticosteroid and thiopyran, herein we intend to develop a simple and efficient strategy to synthesize steroidal thiopyran derivatives starting with different commercially available corticosteroid and study their biological property. Materials and Methods: To achieve our aim, we employed a one-pot multicomponent synthesis of steroidal thiopyran derivatives by the reaction of corticosteriods, malononitrile and carbon disulphide in presence of triethyl amine as a catalyst. Results and Discussion : An array of novel thiopyran compounds were obtained with the highest product yield using Et3N. Scanning electron microscopy analysis manifested agglomeration pertaining to brick - shaped crystals of corticosteroid thiopyran. Synthesized compound were also found to be active as antibacterial agents. Conclusion: We describe a facile one-pot multicomponent synthesis of corticosteroid thiopyran derivatives which are found to possess antibacterial activity. Excellent yields of the products, simple work-up, easily available starting materials and non-chromatographic purification are some main advantages of this protocol.


2019 ◽  
Vol 5 (12) ◽  
pp. eaay1537 ◽  
Author(s):  
Cuibo Liu ◽  
Zhongxin Chen ◽  
Huan Yan ◽  
Shibo Xi ◽  
Kah Meng Yam ◽  
...  

Unprotected E-hydrazone esters are prized building blocks for the preparation of 1H-indazoles and countless other N-containing biologically active molecules. Despite previous advances, efficient and stereoselective synthesis of these compounds remains nontrivial. Here, we show that Pt single atoms anchored on defect-rich CeO2 nanorods (Pt1/CeO2), in conjunction with the alcoholysis of ammonia borane, promotes exceptionally E-selective hydrogenation of α-diazoesters to afford a wide assortment of N-H hydrazone esters with an overall turnover frequency of up to 566 hours−1 upon reaction completion. The α-diazoester substrates could be generated in situ from readily available carboxylic esters in one-pot hydrogenation reaction. Utility is demonstrated through concise, scalable synthesis of 1H-indazole–derived pharmaceuticals and their 15N-labeled analogs. The present protocol highlights a key mechanistic nuance wherein simultaneous coordination of a Pt site with the diazo N═N and ester carbonyl motifs plays a central role in controlling stereoselectivity, which is supported by density functional theory calculations.


2007 ◽  
Vol 15 (23) ◽  
pp. 7311-7317 ◽  
Author(s):  
Dirk Menche ◽  
Fatih Arikan ◽  
Jun Li ◽  
Sven Rudolph ◽  
Florenz Sasse

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2190
Author(s):  
Larisa V. Zhilitskaya ◽  
Bagrat A. Shainyan ◽  
Nina O. Yarosh

The review is devoted to modern trends in the chemistry of 2-amino and 2-mercapto substituted benzothiazoles covering the literature since 2015. The reviewed heterocycles belong to biologically active and industrially demanded compounds. Newly developed synthesis methods can be divided into conventional multistep processes and one-pot, atom economy procedures, realized using green chemistry principles and simple reagents. The easy functionalization of the 2-NH2 and 2-SH groups and the benzene ring of the benzothiazole moiety allows considering them as highly reactive building blocks for organic and organoelement synthesis, including the synthesis of pharmacologically active heterocycles. The review provides a summary of findings, which may be useful for developing new drugs and materials and new synthetic approaches and patterns of reactivity.


2018 ◽  
Vol 69 (03) ◽  
pp. 249-256
Author(s):  
PERDUM ELENA ◽  
MEDVEDOVICI ANDREI VALENTIN ◽  
TACHE FLORENTIN ◽  
VISILEANU EMILIA ◽  
DUMITRESCU IULIANA ◽  
...  

Chemicals safety control and ecological properties have become a priority for the textile industry in order to avoid the negative effects on humans and environment. The increasing interest for toxicology of textiles is determined by the presence of dangerous compounds in clothes generated from dyeing and finishing processes. In order to protect human health, European Regulations as Oeko Tex Standard 100 and REACH Regulation limit the presence of dangerous chemicals, such as aromatic amines, generated by reductive cleavage of azo dyes, by no more than 30 mg/kg of textile material. The main goal of this research work was to develop and validate a HPLC/MWD method for precise and reliable identification and quantification of carcinogenic aromatic amines derived from banned azo dye specific to the textile industry. The simultaneous determination of 24 regulated aromatic amines has been conducted by two chromatographic methods according to SR EN ISO 14362-1:2017 in order to avoid matrix interferences and compounds misidentification due to the presence of structural isomers. Preliminary analyses to establish the maximum absorption wavelength of each standard solution of aromatic amine were performed simultaneously at four wavelengths, 240, 280, 305 and 380 nm. With the scope of demonstrating the consistency, reliability and accuracy of the analysed data, both liquid and gas chromatographic method were validated. Parameters as selectivity, precision, limit of detection and limit of quantification of the analytical methods were evaluated. The certainty of the determinations was also proved by the results of proficiency testing conducted by IIS Netherlands on azo dyes in textiles.


2019 ◽  
Vol 31 (10) ◽  
pp. 2383-2388 ◽  

A simple and efficient method has been employed for synthesis of a novel series of biologically active α-aminophosphonates (4a-j) by reacting 1H-benzo[d]imidazole-2-carbaldehyde (1) and various aromatic amines (2a-j) and diethyl/dimethyl phosphite (3) by Kabachnik-Field's reaction in the presence of efficient heterogeneous K2CO3/Al2O3 catalyst under solvent-free conditions at 140 ºC. Structures of all the compounds were confirmed by 1H, 13C and 31P NMR and LC-MS. In addition to this antioxidant activity were also evaluated.


2020 ◽  
Vol 17 (6) ◽  
pp. 457-463 ◽  
Author(s):  
Sana Sikandar ◽  
Ameer Fawad Zahoor ◽  
Sajjad Ahmad ◽  
Muhammad Naveed Anjum ◽  
Mirza Nadeem Ahmad ◽  
...  

Background: The pyrano[2,3-c]pyrazole derivatives are important building blocks of many biologically active compounds owing to their diverse biological potential for example, anti-inflammatory, anticancer, anti-microbial and anti-oxidant properties. Objective: Keeping in mind the wide range of applications of pyrano[2,3-c]pyrazoles, herein we intended to develop a novel synthetic methodology for dihydropyranopyrazoles. We were also interested in determining the influence of amino acids and dipeptides as a catalyst on the synthesis of pyrano[2,3-c]pyrazole derivatives. Methods: To achieve our objectives, we used a one-pot multi-component reaction of ethyl 3-oxobutanoate, propanedinitrile, hydrazine monohydrate and several substituted benzaldehydes by using different catalysts and solvents to synthesize our desired products in the presence of various catalysts. Results and Discussion: We found that optimal conditions for the preparation of pyrano[2,3-c]pyrazoles were L-cysteine (0.5 mol) in the presence of water:ethanol (9:1) at 90 °C. Various 1,4-dihydropyrano[2,3- c]pyrazoles were afforded by using several substituted benzaldehydes in 66-97% yields. Conclusion: We described a green and environmentally benign method to synthesize pyrano[2,3-c]pyrazoles in a one-pot four component reaction of ethyl 3-oxobutanoate, propanedinitrile, hydrazine monohydrate and different substituted benzaldehyde in the presence of L-cysteine in aqueous ethanol (9:1) at 90 oC. Excellent yields of the products, simple work-up, easily available starting materials, use of green solvents, naturally occurring catalyst, non-toxicity, non-chromatographic purification and environmentally benign reaction conditions are some main advantages of this protocol.


ChemInform ◽  
2008 ◽  
Vol 39 (9) ◽  
Author(s):  
Dirk Menche ◽  
Fatih Arikan ◽  
Jun Li ◽  
Sven Rudolph ◽  
Florenz Sasse

Sign in / Sign up

Export Citation Format

Share Document