Process for the production of fused, tricyclic sulfonamides
The present invention provides methods, i.e., scalable or large-scale processes for the production of fused, tricyclic sulfonamido analogs, such as substituted or unsubstituted 5- (aryl-sulfonyl)-4,5-dihydro- 1-pyrazolo[4,3-c]quinolines and 5-(heteroaryl-sulfonyl)-4,5- dihydro-1-pyrazolo[4,3-c]quino...
Gespeichert in:
Hauptverfasser: | , , , , , , , |
---|---|
Format: | Patent |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | JAGODZINSKI, JACEK J DAPPEN, MICHAEL S LATIMER, LEE H MATUNAS, ROBERT M GODFREY JR., JOLLIE DUAINE PROBST, GARY D WU, JING DRABB, THOMAS W |
description | The present invention provides methods, i.e., scalable or large-scale processes for the production of fused, tricyclic sulfonamido analogs, such as substituted or unsubstituted 5- (aryl-sulfonyl)-4,5-dihydro- 1-pyrazolo[4,3-c]quinolines and 5-(heteroaryl-sulfonyl)-4,5- dihydro-1-pyrazolo[4,3-c]quinolines. Exemplary methods of the invention include an intra-molecular cyclization step, in which a carbon-nitrogen bond is formed, and which employs a copper-based catalyst that contains at least one organic ligand, such as DMEDA. The invention further provides compounds, which are useful as intermediates in the methods of the invention. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_AU2010229954A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>AU2010229954A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_AU2010229954A13</originalsourceid><addsrcrecordid>eNrjZLAOKMpPTi0uVkjLL1IoyUhVKCjKTylNLsnMz1PIT1NIKy1OTdFRKCnKTK5MzslMViguzUnLz0vMzUxJLeZhYE1LzClO5YXS3AzKbq4hzh66qQX58anFBYnJqXmpJfGOoUYGhgZGRpaWpiaOhsbEqQIAeM0wbA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Process for the production of fused, tricyclic sulfonamides</title><source>esp@cenet</source><creator>JAGODZINSKI, JACEK J ; DAPPEN, MICHAEL S ; LATIMER, LEE H ; MATUNAS, ROBERT M ; GODFREY JR., JOLLIE DUAINE ; PROBST, GARY D ; WU, JING ; DRABB, THOMAS W</creator><creatorcontrib>JAGODZINSKI, JACEK J ; DAPPEN, MICHAEL S ; LATIMER, LEE H ; MATUNAS, ROBERT M ; GODFREY JR., JOLLIE DUAINE ; PROBST, GARY D ; WU, JING ; DRABB, THOMAS W</creatorcontrib><description>The present invention provides methods, i.e., scalable or large-scale processes for the production of fused, tricyclic sulfonamido analogs, such as substituted or unsubstituted 5- (aryl-sulfonyl)-4,5-dihydro- 1-pyrazolo[4,3-c]quinolines and 5-(heteroaryl-sulfonyl)-4,5- dihydro-1-pyrazolo[4,3-c]quinolines. Exemplary methods of the invention include an intra-molecular cyclization step, in which a carbon-nitrogen bond is formed, and which employs a copper-based catalyst that contains at least one organic ligand, such as DMEDA. The invention further provides compounds, which are useful as intermediates in the methods of the invention.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>2011</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20111006&DB=EPODOC&CC=AU&NR=2010229954A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20111006&DB=EPODOC&CC=AU&NR=2010229954A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JAGODZINSKI, JACEK J</creatorcontrib><creatorcontrib>DAPPEN, MICHAEL S</creatorcontrib><creatorcontrib>LATIMER, LEE H</creatorcontrib><creatorcontrib>MATUNAS, ROBERT M</creatorcontrib><creatorcontrib>GODFREY JR., JOLLIE DUAINE</creatorcontrib><creatorcontrib>PROBST, GARY D</creatorcontrib><creatorcontrib>WU, JING</creatorcontrib><creatorcontrib>DRABB, THOMAS W</creatorcontrib><title>Process for the production of fused, tricyclic sulfonamides</title><description>The present invention provides methods, i.e., scalable or large-scale processes for the production of fused, tricyclic sulfonamido analogs, such as substituted or unsubstituted 5- (aryl-sulfonyl)-4,5-dihydro- 1-pyrazolo[4,3-c]quinolines and 5-(heteroaryl-sulfonyl)-4,5- dihydro-1-pyrazolo[4,3-c]quinolines. Exemplary methods of the invention include an intra-molecular cyclization step, in which a carbon-nitrogen bond is formed, and which employs a copper-based catalyst that contains at least one organic ligand, such as DMEDA. The invention further provides compounds, which are useful as intermediates in the methods of the invention.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2011</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLAOKMpPTi0uVkjLL1IoyUhVKCjKTylNLsnMz1PIT1NIKy1OTdFRKCnKTK5MzslMViguzUnLz0vMzUxJLeZhYE1LzClO5YXS3AzKbq4hzh66qQX58anFBYnJqXmpJfGOoUYGhgZGRpaWpiaOhsbEqQIAeM0wbA</recordid><startdate>20111006</startdate><enddate>20111006</enddate><creator>JAGODZINSKI, JACEK J</creator><creator>DAPPEN, MICHAEL S</creator><creator>LATIMER, LEE H</creator><creator>MATUNAS, ROBERT M</creator><creator>GODFREY JR., JOLLIE DUAINE</creator><creator>PROBST, GARY D</creator><creator>WU, JING</creator><creator>DRABB, THOMAS W</creator><scope>EVB</scope></search><sort><creationdate>20111006</creationdate><title>Process for the production of fused, tricyclic sulfonamides</title><author>JAGODZINSKI, JACEK J ; DAPPEN, MICHAEL S ; LATIMER, LEE H ; MATUNAS, ROBERT M ; GODFREY JR., JOLLIE DUAINE ; PROBST, GARY D ; WU, JING ; DRABB, THOMAS W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_AU2010229954A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2011</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>JAGODZINSKI, JACEK J</creatorcontrib><creatorcontrib>DAPPEN, MICHAEL S</creatorcontrib><creatorcontrib>LATIMER, LEE H</creatorcontrib><creatorcontrib>MATUNAS, ROBERT M</creatorcontrib><creatorcontrib>GODFREY JR., JOLLIE DUAINE</creatorcontrib><creatorcontrib>PROBST, GARY D</creatorcontrib><creatorcontrib>WU, JING</creatorcontrib><creatorcontrib>DRABB, THOMAS W</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JAGODZINSKI, JACEK J</au><au>DAPPEN, MICHAEL S</au><au>LATIMER, LEE H</au><au>MATUNAS, ROBERT M</au><au>GODFREY JR., JOLLIE DUAINE</au><au>PROBST, GARY D</au><au>WU, JING</au><au>DRABB, THOMAS W</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Process for the production of fused, tricyclic sulfonamides</title><date>2011-10-06</date><risdate>2011</risdate><abstract>The present invention provides methods, i.e., scalable or large-scale processes for the production of fused, tricyclic sulfonamido analogs, such as substituted or unsubstituted 5- (aryl-sulfonyl)-4,5-dihydro- 1-pyrazolo[4,3-c]quinolines and 5-(heteroaryl-sulfonyl)-4,5- dihydro-1-pyrazolo[4,3-c]quinolines. Exemplary methods of the invention include an intra-molecular cyclization step, in which a carbon-nitrogen bond is formed, and which employs a copper-based catalyst that contains at least one organic ligand, such as DMEDA. The invention further provides compounds, which are useful as intermediates in the methods of the invention.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng |
recordid | cdi_epo_espacenet_AU2010229954A1 |
source | esp@cenet |
subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES |
title | Process for the production of fused, tricyclic sulfonamides |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T05%3A34%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=JAGODZINSKI,%20JACEK%20J&rft.date=2011-10-06&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EAU2010229954A1%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |