Syntheses of benzothiazinophenothiazine derivatives and evaluation of their antimicrobial activities
Table Of Contents
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Title page …………………………………………………………………………….i<br>Certification …………………………………………….………………………….ii<br>Dedication ……………………………………………………………………….….iii.<br>Acknowledgement …………………………………………………………….……iv<br>Abstract ……………………………………………………………………………….v<br>List of Figures …………………………………………………………………….…vi<br>List of Tables ……………………………………………………………………….vii<br>Abbreviations ………………………………………………………………….……vii<br>Table of Contents …………………………………….………………………………viii<br>1.0 INTRODUCTION<br>1.1 Background of study …………………………………………………………….1<br>1.2 Statement of problem ……………………………………………………….…..7<br>1.3 Aims and objectives of study ……………………………………………………7<br>1.4 Justification of study ………………………………………………………………8<br>2.0 LITERATURE REVIEW<br>2.1 Linear Phenothiazines ………………………………………………………… 9<br>2.2 Aza-Analogues of Linear Phenothiazines…………………………………….. 15<br>2.3 Angular Phenothiazines……………………………………………………….. 18<br>2.4 Aza-Analogues of Angular Phenothiazines …………………………………… 22<br>2.5 Branched Benzothiazinophenothiazine Ring systems ………………………… 27<br>3.0 EXPERIMENTAL<br>xi<br>3.1 2,4-Diamino-6-hydroxypyrimidine-5-thiol…………………………………….. 37<br>3.2 6-chloro-5H-benzo[a]phenothiazin-5-one ……………………………………………38<br>3.3 7-amino-9-hydroxy-6,8-diazabenzo[a][1,4]benzothiazino[3,2-c]phenothiazine…….. 38<br>3.4 4-amino-2-ethylthio-6-hydroxypyrimidine-5-thiol …………………………………….39<br>3.5 7,14-diethylthio-9,12-dihydroxy-6,8,13,15-tetraazabenzo[a][1,4]benzothiazino[3,2-<br>c]phenothiazine …………………………………………………………………… 40<br>3.6 3-amino-6-methoxypyridine-2-thiol ………………………………………………. 41<br>3.7 8,13-dimethoxy-9,12-diazabenzo[a][1,4]benzothiazino[3,2-c]phenothiazine ……. 47<br>3.8 6,13-dichloro-3,10-diethylthio-1,8-dihydroxy-2,4,9,11-tetrazatriphenodithiazine<br>…………………………………………………………………………………….. 42<br>3.9 4-amino-2-methyl-6-hydroxypyrimidine-5-thiol ………………………………….. 42<br>3.10 6,13-dichloro-3-methyl-9-methoxy-1-hydroxy-2,4,8-triazatriphenodithiazine<br>………………………………………………………………………………………………………………… 43<br>3.11 Evaluation of the Synthesized Phenothiazine Derivatives for Antimicrobial<br>Activities…………………………………………………………………………… 44<br>3.11.1 Sensitivity Test of the Compounds .……………………………………………. 44<br>3.11.2 Determination of Minimum Inhibitory Concentration (MIC) of the<br>Synthesized Derivatives……………………………………………………………. 45<br>4.0 RESULTS AND DISCUSSION<br>4.1 6-chloro-5H-benzo[a]phenothiazin-5-one …………………………………………….. 46<br>4.2 7-amino-9-hydroxy-6,8-diazabenzo[a][1,4]benzothiazino[3,2-c]phenothiazine<br>……………………………………………………………………………………… 48<br>xii<br>4.3 7,14-diethylthio-9,12-dihydroxy-6,8,13,15-tetraazabenzo[a][1,4]benzothiazino[3,2-<br>c]phenothiazine ……………………………………………………………………… 51<br>4.4 8,13-dimethoxy-9,12-diazabenzo[a][1,4]benzothiazino[3,2-<br>c]phenothiazine…………………………………………………………………… 54<br>4.5 6,13-dichloro-3,10-diethylthio-1,8-dihydroxy-2,4,9,11-tetrazatriphenodithiazine…<br>……………………………………………………………………………………. 57<br>4.6 6,13-dichloro-3-methyl-9-methoxy-1-hydroxy-2,4,8-triazatriphenodithiazine<br>…………………………………………………………………………………….. 59<br>4.7 Results of Antimicrobial Sensitivity Test of the Synthesized Compounds………. 62<br>4.8 Results of Inhibition Zones Diameter of the Compound……………………………. 63<br>4.9 Results of Minimum Inhibitory Concentration of the Synthesized Compounds…… 64<br>4.10 Conclusion…………………………………………………………………………… 65<br>REFERENCES ……………………………………………………………………………..66
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Project Abstract
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</p><p>The syntheses of benzothiazinophenothiazine derivatives from simple heterocyclic compounds as<br>precursors is described. Condensation of 2-aminothiophenol with 2,3-dichloro-1,4-naphthoquinone in<br>an alkaline medium furnished a good yield of the intermediate, 6-chloro-5H-benzo[a]phenothiazin-5-<br>one. Further condensation of the intermediate with 2,4-diamino-6-hydroxypyrimidine-5-thiol<br>obtained by alkaline hydrolysis of 2,4-diamino-6-hydroxy-5-thiacyanatopyrimidine gave the<br>benzothiazinophenothiazine ring system. On the other hand, using a facile acid-catalyzed method, the<br>synthesis of some benzothiazinophenothiazine ring systems were achieved with improved yield and<br>lesser reaction time. Structures of the compounds were characterized using UV/Visible<br>spectrophotometry, fourier transform infra red, 1HNMR and 13CNMR spectroscopies and elemental<br>analysis. The antimicrobial properties of the synthesized compounds were determined against<br>Bacillus subtilis, Bacillus cereus, Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli,<br>Klebsiella pneumoniae, Candida albican and Aspergillus niger using agar diffusion technique.<br>Results showed that the complex derivatives were significantly active against the mi</p><p><strong> </strong></p>
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Project Overview
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1.0 INTRODUCTION<br>The chemistry of phenothiazine (1) and its derivatives has been of interest for over a century<br>due to their wide range of applications in drug, agriculture, textile, paint and other related industries.<br>Phenothiazine and its derivatives constitute a pharmaceutically important class of heterocycles with a<br>broad spectrum of pharmacological activity; they are useful in medicine as anticonvulsants,1<br>antitumour agents,2,3 antituberculosis,4 tranquilizers and antimalaria agents5. It also has anthelmintic<br>activity, 6, 7, 8 to mention a few.<br>N<br>S<br>H<br>(1)<br>Notable among the early phenothiazine drugs are Chlorpromazine (2) and promethazine (3) which are<br>broad spectrum tranquilizers with diffuse antipsychotic properties9.<br>N<br>S<br>N<br>H3C CH3<br>Cl N<br>S<br>N<br>CH3<br>H3C CH3<br>(2) (3)<br>2<br>These classes of drugs were the largest and most widely investigated class of neuroleptic agents9.<br>Chlorpromazine, the first commercially produced phenothiazine for the management of psychosis,<br>was also one of the first commercially produced in the phenothiazine series shown to have antituberculosis<br>properties both in vitro and in vivo.10,11 Promethazine and chlorpromazine, clinically<br>useful in the chemotherapy of mental and emotional disturbances has further stimulated an<br>investigation into other phenothiazine derivatives for possible central nervous system<br>(CNS)depressant activity.12,13<br>In the petroleum industry, these compounds are useful as antioxidants in gasoline, petroleum<br>lubricants and stabilizers.14-18 They are used as vat dyes and pigments18-22 in textile and paint<br>industries and in agriculture as insecticides and nematodicides.23,24<br>Since the discovery of the parent ring (1), a lot of structural modifications have been carried<br>out to enhance their pharmacological and biological activities, minimize undesirable effects and open<br>new areas of applications.<br>3<br>Such molecular modifications had yielded derivatives such as (4), (5),25 (6), (7), (8) and (9).26<br>N<br>S<br>H<br>N<br>S<br>H<br>N<br>S<br>H<br>N<br>S<br>H<br>N<br>S<br>H<br>N<br>S<br>H<br>(4)<br>(5)<br>(6)<br>(7) (8)<br>(9)<br>Compounds (4), (6), (7) and (9) are described as angular phenothiazines because of the non-linear<br>arrangement of the ring systems27. They possess fused rings at positions a, c, h and j bonds of the<br>phenothiazine.<br>There are also systems in which two benzene rings are attached to two different positions in the<br>parent compound. Such structures include dibenzo[a,h]phenothiazine28 (10),<br>dibenzo[c,h]phenothiazine29 (11) and dibenzo[a,i]phenothiazine (12).<br>4<br>N<br>S<br>H<br>N<br>S<br>H<br>(10)<br>(11) (12)<br>N<br>S<br>H<br>Branched phenothiazine compounds of the types (13) and (14)30 have been reported.<br>(13)<br>(14)<br>N<br>S N<br>S<br>N<br>S<br>H<br>With regard to the aza analogues of angular phenothiazine compounds, there have been<br>reports on the monoaza, diaza and the triaza derivatives such as (15), (16)31, (17) and (18)<br>respectively<br>5<br>(15) (16)<br>N<br>S<br>H<br>N<br>S<br>H<br>N<br>S<br>H<br>N<br>S<br>H<br>N 2N<br>2N<br>N<br>N<br>N<br>(17)<br>(18)<br>On the search for more aza analogues of angular phenothiazine ring system, the first aza<br>analogues of pyrrolo[3,4-a][1,4]benzothiazino[3,2-c]phenothiazine (19) was reported by Japanese<br>workers32.<br>N<br>S N<br>S<br>N<br>H<br>(19)<br>Okafor and Okoro33 also reported the synthesis of the first three-branched diazaphenothiazine<br>dyes of the type (20).<br>6<br>N<br>S N<br>S<br>N<br>(20) N<br>The diaza (21) and triaza (22) three-branched benzoxazinophenothiazine ring systems were<br>reported by Okafor34 and also reported was the tetraaza analogue (23) of benzothiazinophenothiazine<br>ring system by Ezema.35<br>N<br>O N<br>S<br>N<br>O N<br>S<br>N<br>S N<br>S<br>N<br>N<br>N<br>2N<br>2N<br>2N<br>(21) (22)<br>(23)<br>7<br>Other structures synthesized are the aza and non-aza analogues of dibenzotriphenodithiazine ring<br>systems of the types (24)36 and (25).37<br>N<br>S<br>N N<br>S<br>H H<br>(24)<br>N<br>S<br>S<br>N<br>(25)<br>1.2 Statement of the Problem<br>Owing to the wide range of applications of phenothiazines derivatives with highly improved<br>pharmacological and biological activities, several papers describing the successful synthesis of these<br>derivatives had been reported especially on the angular derivatives including the non-aza and the<br>congeneric aza analogues. However, there are still limited literatures on the complex derivatives of<br>this phenothiazine ring system and, hence, modification of the existing ones is necessary.<br>The past work done was based on their dye and pigment properties. Not much is known of<br>antimicrobial properties of these complex phenothiazine derivatives.<br>1.3 Aims and Objectives of Study<br>The aims and objectives of this study were to:<br>i. Synthesize complex aza derivatives of benzothiazinophenothiazine.<br>ii. Characterize the synthesized compounds by spectral analysis.<br>iii. Undertake antimicrobial screening on the complex derivatives.<br>8<br>1.4 Justification of the Study<br>The wide pharmaceutical applications of phenothiazines and the need to synthesize more<br>derivatives with better and more desirable pharmacological properties led to the synthesis and<br>antimicrobial screening of the derivative undertaken in the present
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