EFFECT OF A LATERAL CHLORO GROUP ON AZOMESOGENS CONTAINING THE NAPHTHALENE MOIETY

Author(s):  
A. K. Prajapati* ◽  
H. M. Pandya
Keyword(s):  
2019 ◽  
Vol 19 (2) ◽  
pp. 146-151
Author(s):  
Vipin Kumar ◽  
Shweta Verma ◽  
Sushil Kumar

Background: Approach for green chemistry for chemical synthesis is found to be very efficient as it makes the reaction more easily, less tedious, maximize desired products and minimize by-products. Materials & Methods: Utilizing this approach 1, 5-benzodiazepines and its derivatives have been synthesized and evaluated for skeletal muscle and antianxiety activity. 1, 5-benzodiazepine derivatives have attracted great attention due to its diversity of pharmacological activities and its application in heterocyclic synthesis and medicines. The target compounds were synthesized by first reacting o-phenylenediamine with acetophenone to yield 1, 5-benzodiazepines. In the next step the NH of 1, 5-benzodiazepines were chloroacetylated and then the chloro group was substituted with different anilines. The structures were confirmed on the basis of their TLC, IR, 1H NMR and CHN elemental studies. The physicochemical parameters were determined for BBB penetration through online software. Results: The Log P values of the compounds tested showed that compounds have the potential to be CNS active. The compounds were evaluated for the skeletal muscle relaxant activity and antianxiety activity. It was investigated that 1, 5-benzodiazepines derivatives possess significant differences between control group and treated group. Conclusion: Among these derivatives, the compound bearing chloro group possesses the highest skeletal muscle relaxant and antianxiety activity.


ACS Omega ◽  
2018 ◽  
Vol 3 (10) ◽  
pp. 13790-13797 ◽  
Author(s):  
Keiki Sakurama ◽  
Akito Kawai ◽  
Victor Tuan Giam Chuang ◽  
Yoko Kanamori ◽  
Miyu Osa ◽  
...  

2019 ◽  
Vol 6 (11) ◽  
pp. 190562 ◽  
Author(s):  
Qingming Zhang ◽  
Hongyu Liu ◽  
Muhammad Saleem ◽  
Caixia Wang

Chlorothalonil is a widely used fungicide, but the contamination of soil and water environments by this chemical causes potential threats to biodiversity. Given the metabolic potential of soil microorganisms, there is a need for developing microbiological approaches to degrade persistent compounds, such as chlorothalonil, in contaminated sites. Here in this study, we isolated a bacterial strain (namely, BJ1) capable of degrading chlorothalonil from a chlorothalonil-contaminated farmland soil in the Shandong Province, China. Using 16S rDNA gene sequencing, morphological and biological characteristics, we identified the strain BJ1 as Stenotrophomonas acidaminiphila . The strain BJ1 uses chlorothalonil as a sole carbon source. At initial concentrations of 50, 100, 200 and 300 mg l −1 , it degraded 91.5%, 89.4%, 86.5% and 83.5% of chlorothalonil after 96 h of inoculation under optimum conditions (30°C and pH 7.0). Two metabolites, methyl-2,5,6-trichloro-3-cyano-4-methoxy-benzoate and methyl-3-cyano-2,4,5,6-tetrachlorobenzoate, were detected and identified based on HPLC–MS analysis, which suggests that the strain BJ1 metabolized chlorothalonil through the hydroxylation of chloro-group and hydration of cyano-group. The results of this study highlight the great potential for this bacterium to be used in chlorothalonil pollution remediation.


1992 ◽  
Vol 65 (8) ◽  
pp. 2312-2314 ◽  
Author(s):  
Vishwakarma Singh ◽  
Akio Furusaki ◽  
Carlos Jaime ◽  
Takeshi Matsumoto ◽  
Eiji Osawa
Keyword(s):  

1968 ◽  
Vol 90 (26) ◽  
pp. 7363-7364 ◽  
Author(s):  
P. S. Zacharias ◽  
B. Behera ◽  
Animesh. Chakravorty
Keyword(s):  

1989 ◽  
Vol 67 (10) ◽  
pp. 1618-1623 ◽  
Author(s):  
Alaa S. Abd-El-Aziz ◽  
Adam Piórko ◽  
Choi Chuck Lee ◽  
Ronald G. Sutherland

Nucleophilic substitution reactions of the (η6-o-, -m-, or -p-chloronitrobenzene)(η5-cyclopentadienyl)iron cation (2a, 2b, or 2c, respectively) with aniline, n-butylamine, or pyrrolidine as nucleophile were investigated. It was found that only selective displacement of the nitro group occurred for reactions with aniline. For reaction with n-butylamine or pyrrolidine, o-isomer 2a resulted in the selective displacement of only the chloro group, giving rise to the (η6-o-n-butylaminonitrobenzene)(η5-cyclo-pentadienyl)iron cation (5a) or the (η6-o-nitro-N-pyrrolidinylbenzene)(η5-cyclopentadienyl)iron cation (7a), respectively. With the m- or p-isomer 2b or 2c, reaction with n-butylamine or pyrrolidine gave a mixture of substitution products from competitive displacements of both chloro and nitro groups, the major product from the m-isomer being derived from displacement of the chloro group while the major product from the p-isomer resulted from displacement of the nitro group. Possible interpretations of these results on the basis that the basicity of the nucleophile and the combined inductive effects of the nitro and chloro substituents would play important roles are presented. Keywords: (η6-o-, -m-, and -p-chloronitrobenzene)(η5-cyclopentadienyl)iron cations, nucleophilic substitution reactions, aniline, n-butylamine, pyrrolidine.


2014 ◽  
Vol 26 (9) ◽  
pp. 2733-2735
Author(s):  
Ruo-Yan Li ◽  
Li Jing ◽  
Jiao-Long Meng ◽  
Gang Li

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