Loading…

Novel synthesis, ring transformation and anticancer activity of 1,3-thiazine, pyrimidine and triazolo[1,5-a]pyrimidine derivatives

Synthesis, heterocyclization and anticancer activity of a new series of heterocyclic compounds are described. Aminothiazine 1 was obtained from the base induced condensation of thiourea, benzaldehyde and ethyl cyanoacetate. The synthesis of N-phenyl amino pyrimidine derivative 2 was obtained as a re...

Full description

Saved in:
Bibliographic Details
Published in:Bulletin of the Chemical Society of Ethiopia 2018-01, Vol.32 (3), p.513
Main Authors: Sayed, Hassan A. El, Hashash, Maher M. El, Ahmed, Aiada E
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c276t-c346d2886216d15676cebf57e0067ac439de1448ad8f3b27dfac1604dbe287af3
cites
container_end_page
container_issue 3
container_start_page 513
container_title Bulletin of the Chemical Society of Ethiopia
container_volume 32
creator Sayed, Hassan A. El
Hashash, Maher M. El
Ahmed, Aiada E
description Synthesis, heterocyclization and anticancer activity of a new series of heterocyclic compounds are described. Aminothiazine 1 was obtained from the base induced condensation of thiourea, benzaldehyde and ethyl cyanoacetate. The synthesis of N-phenyl amino pyrimidine derivative 2 was obtained as a result of reaction of aniline with compound 1. Compound 2 underwent ring opening and recyclization upon reaction with HCl or [H.sub.2][O.sub.2]/NaOH to afford the acid derivative 3 or oxazine 4, respectively. Thiazine 1 undergoes ring transformation upon the effect of N[H.sub.2]OH*HCl to produce pyrimidine derivative 5. Heterocyclization of compound 1 with thiosemicarbazide followed by oxidation with [I.sub.2]/AcOH afforded triazolopyrimidine 6 and 7, respectively. Alkylation of compound 1 was promoted by reaction of 1 with ethyl iodide to give alkylated thiazine 8 which in turn undergo ring transformation when subjected to reaction with hydrazine hydrate to give pyrazole derivative 9. Refluxing of amino-1,3-thiazine derivative 1 with ethyl bromoacetate in the presence of [Et.sub.3]N produce the alkylated pyrimidine product 10. Hydrazonolysis of 1,3-thiazine 1 with hydrazine or phenyhydrazine gave pyrimidine derivatives 11a,b, respectively. Compound 11b was cyclized with carbon disulfide or formaldehyde to produce triazolopyrimidines 12 and 13, respectively. Some of the new compounds were screened for anticancer activity and significant results were found for some compounds.KEY WORDS: 1,3-Thiazine, Pyrimidine, Triazole, Pyrazole, Anticancer activity
doi_str_mv 10.4314/bcse.v32i3.10
format article
fullrecord <record><control><sourceid>gale_cross</sourceid><recordid>TN_cdi_gale_infotracacademiconefile_A566682102</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A566682102</galeid><sourcerecordid>A566682102</sourcerecordid><originalsourceid>FETCH-LOGICAL-c276t-c346d2886216d15676cebf57e0067ac439de1448ad8f3b27dfac1604dbe287af3</originalsourceid><addsrcrecordid>eNpNUMtqwzAQFKWFpo9j7_4Ay9XLsnMMoS8I7aWFQilG1iNRcaQgCYN77JdXSXooy7LDLDPsDgA3GFWMYnbby6irkRJLK4xOwAw3hMMW4ffTjBHGkM4JOwcXMX4hRBBt6hn4efajHoo4ubTR0cayCNatixSEi8aHrUjWu0I4lTtZKZzUoRAy2dGmqfCmwCWFaWPFt3W6LHZTsFurMj5oUsgLP_gPXNZQfP7bKh3smM1HHa_AmRFD1Nd_8xK83d-9Lh_h6uXhablYQUkanqCkjCvStpxgrnDNGy51b-pGI8QbIRmdK40Za4VqDe1Jo4yQmCOmek3aRhh6Caqj71oMurPO-PylzKX01krvtLGZX9Sc85ZgRLIAHgUy-BiDNt0u3y_C1GHU7RPv9ol3h8QzRX8BjIJ4Mw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Novel synthesis, ring transformation and anticancer activity of 1,3-thiazine, pyrimidine and triazolo[1,5-a]pyrimidine derivatives</title><source>Free Full-Text Journals in Chemistry</source><creator>Sayed, Hassan A. El ; Hashash, Maher M. El ; Ahmed, Aiada E</creator><creatorcontrib>Sayed, Hassan A. El ; Hashash, Maher M. El ; Ahmed, Aiada E</creatorcontrib><description>Synthesis, heterocyclization and anticancer activity of a new series of heterocyclic compounds are described. Aminothiazine 1 was obtained from the base induced condensation of thiourea, benzaldehyde and ethyl cyanoacetate. The synthesis of N-phenyl amino pyrimidine derivative 2 was obtained as a result of reaction of aniline with compound 1. Compound 2 underwent ring opening and recyclization upon reaction with HCl or [H.sub.2][O.sub.2]/NaOH to afford the acid derivative 3 or oxazine 4, respectively. Thiazine 1 undergoes ring transformation upon the effect of N[H.sub.2]OH*HCl to produce pyrimidine derivative 5. Heterocyclization of compound 1 with thiosemicarbazide followed by oxidation with [I.sub.2]/AcOH afforded triazolopyrimidine 6 and 7, respectively. Alkylation of compound 1 was promoted by reaction of 1 with ethyl iodide to give alkylated thiazine 8 which in turn undergo ring transformation when subjected to reaction with hydrazine hydrate to give pyrazole derivative 9. Refluxing of amino-1,3-thiazine derivative 1 with ethyl bromoacetate in the presence of [Et.sub.3]N produce the alkylated pyrimidine product 10. Hydrazonolysis of 1,3-thiazine 1 with hydrazine or phenyhydrazine gave pyrimidine derivatives 11a,b, respectively. Compound 11b was cyclized with carbon disulfide or formaldehyde to produce triazolopyrimidines 12 and 13, respectively. Some of the new compounds were screened for anticancer activity and significant results were found for some compounds.KEY WORDS: 1,3-Thiazine, Pyrimidine, Triazole, Pyrazole, Anticancer activity</description><identifier>ISSN: 1011-3924</identifier><identifier>EISSN: 1726-801X</identifier><identifier>DOI: 10.4314/bcse.v32i3.10</identifier><language>eng</language><publisher>Chemical Society of Ethiopia</publisher><subject>Chemical properties ; Chemical synthesis ; Methods ; Production processes ; Pyrimidines</subject><ispartof>Bulletin of the Chemical Society of Ethiopia, 2018-01, Vol.32 (3), p.513</ispartof><rights>COPYRIGHT 2018 Chemical Society of Ethiopia</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c276t-c346d2886216d15676cebf57e0067ac439de1448ad8f3b27dfac1604dbe287af3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sayed, Hassan A. El</creatorcontrib><creatorcontrib>Hashash, Maher M. El</creatorcontrib><creatorcontrib>Ahmed, Aiada E</creatorcontrib><title>Novel synthesis, ring transformation and anticancer activity of 1,3-thiazine, pyrimidine and triazolo[1,5-a]pyrimidine derivatives</title><title>Bulletin of the Chemical Society of Ethiopia</title><description>Synthesis, heterocyclization and anticancer activity of a new series of heterocyclic compounds are described. Aminothiazine 1 was obtained from the base induced condensation of thiourea, benzaldehyde and ethyl cyanoacetate. The synthesis of N-phenyl amino pyrimidine derivative 2 was obtained as a result of reaction of aniline with compound 1. Compound 2 underwent ring opening and recyclization upon reaction with HCl or [H.sub.2][O.sub.2]/NaOH to afford the acid derivative 3 or oxazine 4, respectively. Thiazine 1 undergoes ring transformation upon the effect of N[H.sub.2]OH*HCl to produce pyrimidine derivative 5. Heterocyclization of compound 1 with thiosemicarbazide followed by oxidation with [I.sub.2]/AcOH afforded triazolopyrimidine 6 and 7, respectively. Alkylation of compound 1 was promoted by reaction of 1 with ethyl iodide to give alkylated thiazine 8 which in turn undergo ring transformation when subjected to reaction with hydrazine hydrate to give pyrazole derivative 9. Refluxing of amino-1,3-thiazine derivative 1 with ethyl bromoacetate in the presence of [Et.sub.3]N produce the alkylated pyrimidine product 10. Hydrazonolysis of 1,3-thiazine 1 with hydrazine or phenyhydrazine gave pyrimidine derivatives 11a,b, respectively. Compound 11b was cyclized with carbon disulfide or formaldehyde to produce triazolopyrimidines 12 and 13, respectively. Some of the new compounds were screened for anticancer activity and significant results were found for some compounds.KEY WORDS: 1,3-Thiazine, Pyrimidine, Triazole, Pyrazole, Anticancer activity</description><subject>Chemical properties</subject><subject>Chemical synthesis</subject><subject>Methods</subject><subject>Production processes</subject><subject>Pyrimidines</subject><issn>1011-3924</issn><issn>1726-801X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpNUMtqwzAQFKWFpo9j7_4Ay9XLsnMMoS8I7aWFQilG1iNRcaQgCYN77JdXSXooy7LDLDPsDgA3GFWMYnbby6irkRJLK4xOwAw3hMMW4ffTjBHGkM4JOwcXMX4hRBBt6hn4efajHoo4ubTR0cayCNatixSEi8aHrUjWu0I4lTtZKZzUoRAy2dGmqfCmwCWFaWPFt3W6LHZTsFurMj5oUsgLP_gPXNZQfP7bKh3smM1HHa_AmRFD1Nd_8xK83d-9Lh_h6uXhablYQUkanqCkjCvStpxgrnDNGy51b-pGI8QbIRmdK40Za4VqDe1Jo4yQmCOmek3aRhh6Caqj71oMurPO-PylzKX01krvtLGZX9Sc85ZgRLIAHgUy-BiDNt0u3y_C1GHU7RPv9ol3h8QzRX8BjIJ4Mw</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Sayed, Hassan A. El</creator><creator>Hashash, Maher M. El</creator><creator>Ahmed, Aiada E</creator><general>Chemical Society of Ethiopia</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20180101</creationdate><title>Novel synthesis, ring transformation and anticancer activity of 1,3-thiazine, pyrimidine and triazolo[1,5-a]pyrimidine derivatives</title><author>Sayed, Hassan A. El ; Hashash, Maher M. El ; Ahmed, Aiada E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c276t-c346d2886216d15676cebf57e0067ac439de1448ad8f3b27dfac1604dbe287af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Chemical properties</topic><topic>Chemical synthesis</topic><topic>Methods</topic><topic>Production processes</topic><topic>Pyrimidines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sayed, Hassan A. El</creatorcontrib><creatorcontrib>Hashash, Maher M. El</creatorcontrib><creatorcontrib>Ahmed, Aiada E</creatorcontrib><collection>CrossRef</collection><jtitle>Bulletin of the Chemical Society of Ethiopia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sayed, Hassan A. El</au><au>Hashash, Maher M. El</au><au>Ahmed, Aiada E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel synthesis, ring transformation and anticancer activity of 1,3-thiazine, pyrimidine and triazolo[1,5-a]pyrimidine derivatives</atitle><jtitle>Bulletin of the Chemical Society of Ethiopia</jtitle><date>2018-01-01</date><risdate>2018</risdate><volume>32</volume><issue>3</issue><spage>513</spage><pages>513-</pages><issn>1011-3924</issn><eissn>1726-801X</eissn><abstract>Synthesis, heterocyclization and anticancer activity of a new series of heterocyclic compounds are described. Aminothiazine 1 was obtained from the base induced condensation of thiourea, benzaldehyde and ethyl cyanoacetate. The synthesis of N-phenyl amino pyrimidine derivative 2 was obtained as a result of reaction of aniline with compound 1. Compound 2 underwent ring opening and recyclization upon reaction with HCl or [H.sub.2][O.sub.2]/NaOH to afford the acid derivative 3 or oxazine 4, respectively. Thiazine 1 undergoes ring transformation upon the effect of N[H.sub.2]OH*HCl to produce pyrimidine derivative 5. Heterocyclization of compound 1 with thiosemicarbazide followed by oxidation with [I.sub.2]/AcOH afforded triazolopyrimidine 6 and 7, respectively. Alkylation of compound 1 was promoted by reaction of 1 with ethyl iodide to give alkylated thiazine 8 which in turn undergo ring transformation when subjected to reaction with hydrazine hydrate to give pyrazole derivative 9. Refluxing of amino-1,3-thiazine derivative 1 with ethyl bromoacetate in the presence of [Et.sub.3]N produce the alkylated pyrimidine product 10. Hydrazonolysis of 1,3-thiazine 1 with hydrazine or phenyhydrazine gave pyrimidine derivatives 11a,b, respectively. Compound 11b was cyclized with carbon disulfide or formaldehyde to produce triazolopyrimidines 12 and 13, respectively. Some of the new compounds were screened for anticancer activity and significant results were found for some compounds.KEY WORDS: 1,3-Thiazine, Pyrimidine, Triazole, Pyrazole, Anticancer activity</abstract><pub>Chemical Society of Ethiopia</pub><doi>10.4314/bcse.v32i3.10</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1011-3924
ispartof Bulletin of the Chemical Society of Ethiopia, 2018-01, Vol.32 (3), p.513
issn 1011-3924
1726-801X
language eng
recordid cdi_gale_infotracacademiconefile_A566682102
source Free Full-Text Journals in Chemistry
subjects Chemical properties
Chemical synthesis
Methods
Production processes
Pyrimidines
title Novel synthesis, ring transformation and anticancer activity of 1,3-thiazine, pyrimidine and triazolo[1,5-a]pyrimidine derivatives
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T11%3A31%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20synthesis,%20ring%20transformation%20and%20anticancer%20activity%20of%201,3-thiazine,%20pyrimidine%20and%20triazolo%5B1,5-a%5Dpyrimidine%20derivatives&rft.jtitle=Bulletin%20of%20the%20Chemical%20Society%20of%20Ethiopia&rft.au=Sayed,%20Hassan%20A.%20El&rft.date=2018-01-01&rft.volume=32&rft.issue=3&rft.spage=513&rft.pages=513-&rft.issn=1011-3924&rft.eissn=1726-801X&rft_id=info:doi/10.4314/bcse.v32i3.10&rft_dat=%3Cgale_cross%3EA566682102%3C/gale_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c276t-c346d2886216d15676cebf57e0067ac439de1448ad8f3b27dfac1604dbe287af3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A566682102&rfr_iscdi=true