4‑Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications

A number of metathesis reactions were successfully conducted in 4-methyltetrahydropyran, including both standard model dienes, as well as more complex substrates, such as analogues of biologically active compounds and active pharmaceutical ingredients. To place this solvent in a context of pharmaceu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ACS sustainable chemistry & engineering 2020-12, Vol.8 (49), p.18215-18223
Hauptverfasser: Nienałtowski, Tomasz, Krzesiński, Paweł, Baumert, Marcel E, Skoczeń, Aleksandra, Suska-Kauf, Ewa, Pawłowska, Jolanta, Kajetanowicz, Anna, Grela, Karol
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 18223
container_issue 49
container_start_page 18215
container_title ACS sustainable chemistry & engineering
container_volume 8
creator Nienałtowski, Tomasz
Krzesiński, Paweł
Baumert, Marcel E
Skoczeń, Aleksandra
Suska-Kauf, Ewa
Pawłowska, Jolanta
Kajetanowicz, Anna
Grela, Karol
description A number of metathesis reactions were successfully conducted in 4-methyltetrahydropyran, including both standard model dienes, as well as more complex substrates, such as analogues of biologically active compounds and active pharmaceutical ingredients. To place this solvent in a context of pharmaceutical R + D, larger-scale syntheses of SUAM 1221, a prolyl endopeptidase inhibitor with potential application in Alzheimer disease treatment, and a derivative of sildenafil, an analogue of the popular Viagra drug, were executed. In the latter case, despite all the setup being made in air, the metathesis reaction at a 33 g scale proceeded very well with relatively low catalyst loading and without need of aqueous workup or column chromatography.
doi_str_mv 10.1021/acssuschemeng.0c06668
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7739489</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2471535198</sourcerecordid><originalsourceid>FETCH-LOGICAL-a453t-3b85baf443af5b922fc46f0fbe03ac1099e2994ed176b9576c6c03baf88d586a3</originalsourceid><addsrcrecordid>eNqFkc1u1DAUhSMEolXpI4C8ZDPFjp3EYYE0GpUfqVUlCmvrxrlpXHnsYDsjZccjwCvyJHg0Q9Wu8MaW_Z3je3SK4jWjF4yW7B3oGOeoR9yiu7ugmtZ1LZ8VpyWr5YoKWT1_dD4pzmO8p3m1LS8le1mccM6FoK08LX6JPz9_X2MaF5swBRiXPvhpCeAIRAJk490OnUGXyDoTwUEyOyS33u72d4MP5MbiYBzJJpBGjCaSrwg6Ge_ek2vfoyW3ae4NZjvXZ6w32jiwZJPHNzGFhaynyRoNe0l8VbwYwEY8P-5nxfePl982n1dXN5--bNZXKxAVTyveyaqDQQgOQ9W1ZTloUQ906JBy0CxHxbJtBfasqbu2ampda8qzQsq-kjXws-LDwXeauy32OqcJYNUUzBbCojwY9fTFmVHd-Z1qGt4K2WaDt0eD4H_MGJPKaTRaCw79HFUpGlbxirUyo9UB1cHHGHB4-IZRtS9UPSlUHQvNujePZ3xQ_asvA-wAZL2693Oux8b_mP4FbSe3aQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2471535198</pqid></control><display><type>article</type><title>4‑Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications</title><source>American Chemical Society Journals</source><creator>Nienałtowski, Tomasz ; Krzesiński, Paweł ; Baumert, Marcel E ; Skoczeń, Aleksandra ; Suska-Kauf, Ewa ; Pawłowska, Jolanta ; Kajetanowicz, Anna ; Grela, Karol</creator><creatorcontrib>Nienałtowski, Tomasz ; Krzesiński, Paweł ; Baumert, Marcel E ; Skoczeń, Aleksandra ; Suska-Kauf, Ewa ; Pawłowska, Jolanta ; Kajetanowicz, Anna ; Grela, Karol</creatorcontrib><description>A number of metathesis reactions were successfully conducted in 4-methyltetrahydropyran, including both standard model dienes, as well as more complex substrates, such as analogues of biologically active compounds and active pharmaceutical ingredients. To place this solvent in a context of pharmaceutical R + D, larger-scale syntheses of SUAM 1221, a prolyl endopeptidase inhibitor with potential application in Alzheimer disease treatment, and a derivative of sildenafil, an analogue of the popular Viagra drug, were executed. In the latter case, despite all the setup being made in air, the metathesis reaction at a 33 g scale proceeded very well with relatively low catalyst loading and without need of aqueous workup or column chromatography.</description><identifier>ISSN: 2168-0485</identifier><identifier>EISSN: 2168-0485</identifier><identifier>DOI: 10.1021/acssuschemeng.0c06668</identifier><identifier>PMID: 33344098</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>ACS sustainable chemistry &amp; engineering, 2020-12, Vol.8 (49), p.18215-18223</ispartof><rights>2020 American Chemical Society</rights><rights>2020 American Chemical Society.</rights><rights>2020 American Chemical Society 2020 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a453t-3b85baf443af5b922fc46f0fbe03ac1099e2994ed176b9576c6c03baf88d586a3</citedby><cites>FETCH-LOGICAL-a453t-3b85baf443af5b922fc46f0fbe03ac1099e2994ed176b9576c6c03baf88d586a3</cites><orcidid>0000-0003-0315-0998 ; 0000-0002-0625-1906 ; 0000-0001-9193-3305</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acssuschemeng.0c06668$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acssuschemeng.0c06668$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33344098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nienałtowski, Tomasz</creatorcontrib><creatorcontrib>Krzesiński, Paweł</creatorcontrib><creatorcontrib>Baumert, Marcel E</creatorcontrib><creatorcontrib>Skoczeń, Aleksandra</creatorcontrib><creatorcontrib>Suska-Kauf, Ewa</creatorcontrib><creatorcontrib>Pawłowska, Jolanta</creatorcontrib><creatorcontrib>Kajetanowicz, Anna</creatorcontrib><creatorcontrib>Grela, Karol</creatorcontrib><title>4‑Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications</title><title>ACS sustainable chemistry &amp; engineering</title><addtitle>ACS Sustainable Chem. Eng</addtitle><description>A number of metathesis reactions were successfully conducted in 4-methyltetrahydropyran, including both standard model dienes, as well as more complex substrates, such as analogues of biologically active compounds and active pharmaceutical ingredients. To place this solvent in a context of pharmaceutical R + D, larger-scale syntheses of SUAM 1221, a prolyl endopeptidase inhibitor with potential application in Alzheimer disease treatment, and a derivative of sildenafil, an analogue of the popular Viagra drug, were executed. In the latter case, despite all the setup being made in air, the metathesis reaction at a 33 g scale proceeded very well with relatively low catalyst loading and without need of aqueous workup or column chromatography.</description><issn>2168-0485</issn><issn>2168-0485</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1DAUhSMEolXpI4C8ZDPFjp3EYYE0GpUfqVUlCmvrxrlpXHnsYDsjZccjwCvyJHg0Q9Wu8MaW_Z3je3SK4jWjF4yW7B3oGOeoR9yiu7ugmtZ1LZ8VpyWr5YoKWT1_dD4pzmO8p3m1LS8le1mccM6FoK08LX6JPz9_X2MaF5swBRiXPvhpCeAIRAJk490OnUGXyDoTwUEyOyS33u72d4MP5MbiYBzJJpBGjCaSrwg6Ge_ek2vfoyW3ae4NZjvXZ6w32jiwZJPHNzGFhaynyRoNe0l8VbwYwEY8P-5nxfePl982n1dXN5--bNZXKxAVTyveyaqDQQgOQ9W1ZTloUQ906JBy0CxHxbJtBfasqbu2ampda8qzQsq-kjXws-LDwXeauy32OqcJYNUUzBbCojwY9fTFmVHd-Z1qGt4K2WaDt0eD4H_MGJPKaTRaCw79HFUpGlbxirUyo9UB1cHHGHB4-IZRtS9UPSlUHQvNujePZ3xQ_asvA-wAZL2693Oux8b_mP4FbSe3aQ</recordid><startdate>20201214</startdate><enddate>20201214</enddate><creator>Nienałtowski, Tomasz</creator><creator>Krzesiński, Paweł</creator><creator>Baumert, Marcel E</creator><creator>Skoczeń, Aleksandra</creator><creator>Suska-Kauf, Ewa</creator><creator>Pawłowska, Jolanta</creator><creator>Kajetanowicz, Anna</creator><creator>Grela, Karol</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0315-0998</orcidid><orcidid>https://orcid.org/0000-0002-0625-1906</orcidid><orcidid>https://orcid.org/0000-0001-9193-3305</orcidid></search><sort><creationdate>20201214</creationdate><title>4‑Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications</title><author>Nienałtowski, Tomasz ; Krzesiński, Paweł ; Baumert, Marcel E ; Skoczeń, Aleksandra ; Suska-Kauf, Ewa ; Pawłowska, Jolanta ; Kajetanowicz, Anna ; Grela, Karol</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a453t-3b85baf443af5b922fc46f0fbe03ac1099e2994ed176b9576c6c03baf88d586a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nienałtowski, Tomasz</creatorcontrib><creatorcontrib>Krzesiński, Paweł</creatorcontrib><creatorcontrib>Baumert, Marcel E</creatorcontrib><creatorcontrib>Skoczeń, Aleksandra</creatorcontrib><creatorcontrib>Suska-Kauf, Ewa</creatorcontrib><creatorcontrib>Pawłowska, Jolanta</creatorcontrib><creatorcontrib>Kajetanowicz, Anna</creatorcontrib><creatorcontrib>Grela, Karol</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ACS sustainable chemistry &amp; engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nienałtowski, Tomasz</au><au>Krzesiński, Paweł</au><au>Baumert, Marcel E</au><au>Skoczeń, Aleksandra</au><au>Suska-Kauf, Ewa</au><au>Pawłowska, Jolanta</au><au>Kajetanowicz, Anna</au><au>Grela, Karol</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>4‑Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications</atitle><jtitle>ACS sustainable chemistry &amp; engineering</jtitle><addtitle>ACS Sustainable Chem. Eng</addtitle><date>2020-12-14</date><risdate>2020</risdate><volume>8</volume><issue>49</issue><spage>18215</spage><epage>18223</epage><pages>18215-18223</pages><issn>2168-0485</issn><eissn>2168-0485</eissn><abstract>A number of metathesis reactions were successfully conducted in 4-methyltetrahydropyran, including both standard model dienes, as well as more complex substrates, such as analogues of biologically active compounds and active pharmaceutical ingredients. To place this solvent in a context of pharmaceutical R + D, larger-scale syntheses of SUAM 1221, a prolyl endopeptidase inhibitor with potential application in Alzheimer disease treatment, and a derivative of sildenafil, an analogue of the popular Viagra drug, were executed. In the latter case, despite all the setup being made in air, the metathesis reaction at a 33 g scale proceeded very well with relatively low catalyst loading and without need of aqueous workup or column chromatography.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>33344098</pmid><doi>10.1021/acssuschemeng.0c06668</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-0315-0998</orcidid><orcidid>https://orcid.org/0000-0002-0625-1906</orcidid><orcidid>https://orcid.org/0000-0001-9193-3305</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2168-0485
ispartof ACS sustainable chemistry & engineering, 2020-12, Vol.8 (49), p.18215-18223
issn 2168-0485
2168-0485
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7739489
source American Chemical Society Journals
title 4‑Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T16%3A04%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=4%E2%80%91Methyltetrahydropyran%20as%20a%20Convenient%20Alternative%20Solvent%20for%20Olefin%20Metathesis%20Reaction:%20Model%20Studies%20and%20Medicinal%20Chemistry%20Applications&rft.jtitle=ACS%20sustainable%20chemistry%20&%20engineering&rft.au=Niena%C5%82towski,%20Tomasz&rft.date=2020-12-14&rft.volume=8&rft.issue=49&rft.spage=18215&rft.epage=18223&rft.pages=18215-18223&rft.issn=2168-0485&rft.eissn=2168-0485&rft_id=info:doi/10.1021/acssuschemeng.0c06668&rft_dat=%3Cproquest_pubme%3E2471535198%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2471535198&rft_id=info:pmid/33344098&rfr_iscdi=true