SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-N,N'-SULFONYLHARNSTOFFE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG IN ARZNEIMITTELN

Substituted (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas can be prepared by reaction of (quinolin-2-ylmethoxy)phenylamines with sulphonyl isocyanates, or by reaction of appropriately protected hydroxyanilines with sulphonyl isocyanates and then, after removal of the protective group, with h...

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Hauptverfasser:	MUELLER-PEDDINGHAUS, REINER, DR, RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE, KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE, THEISEN, PIA-OEC.TROP.., 5060 BERGISCH GLADBACH, DE, FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE, MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE
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Sprache:	ger
Schlagworte:	CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
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creator	MUELLER-PEDDINGHAUS, REINER, DR RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE THEISEN, PIA-OEC.TROP.., 5060 BERGISCH GLADBACH, DE FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE
description	Substituted (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas can be prepared by reaction of (quinolin-2-ylmethoxy)phenylamines with sulphonyl isocyanates, or by reaction of appropriately protected hydroxyanilines with sulphonyl isocyanates and then, after removal of the protective group, with halomethylquinolines, or by reaction of (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas with sulphonyl halides. The substituted (quinolin-2-ylmethoxy)phenyl- N,N'-sulphonylureas can be employed as active substances in medicaments, in particular as lipoxygenase inhibitors.
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DR., 5042 ERFTSTADT, DE ; THEISEN, PIA-OEC.TROP.., 5060 BERGISCH GLADBACH, DE ; FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE ; MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE</creator><creatorcontrib>MUELLER-PEDDINGHAUS, REINER, DR ; RADDATZ, SIEGFRIED. DR., 5000 KOELN, DE ; KOHLSDORFER, CHRISTIAN-BIOL. DR., 5042 ERFTSTADT, DE ; THEISEN, PIA-OEC.TROP.., 5060 BERGISCH GLADBACH, DE ; FRUCHTMANN, ROMANIS-BIOL., 5000 KOELN, DE ; MOHRS, KLAUS. DR., 5600 WUPPERTAL, DE</creatorcontrib><description>Substituted (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas can be prepared by reaction of (quinolin-2-ylmethoxy)phenylamines with sulphonyl isocyanates, or by reaction of appropriately protected hydroxyanilines with sulphonyl isocyanates and then, after removal of the protective group, with halomethylquinolines, or by reaction of (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas with sulphonyl halides. The substituted (quinolin-2-ylmethoxy)phenyl- N,N'-sulphonylureas can be employed as active substances in medicaments, in particular as lipoxygenase inhibitors.</description><language>ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1990</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=19900920&DB=EPODOC&CC=DE&NR=3908298A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19900920&DB=EPODOC&CC=DE&NR=3908298A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MUELLER-PEDDINGHAUS, REINER, DR</creatorcontrib><creatorcontrib>RADDATZ, SIEGFRIED. 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DR., 5600 WUPPERTAL, DE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-N,N'-SULFONYLHARNSTOFFE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG IN ARZNEIMITTELN</title><date>1990-09-20</date><risdate>1990</risdate><abstract>Substituted (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas can be prepared by reaction of (quinolin-2-ylmethoxy)phenylamines with sulphonyl isocyanates, or by reaction of appropriately protected hydroxyanilines with sulphonyl isocyanates and then, after removal of the protective group, with halomethylquinolines, or by reaction of (quinolin-2-ylmethoxy)phenyl-N,N'-sulphonylureas with sulphonyl halides. The substituted (quinolin-2-ylmethoxy)phenyl- N,N'-sulphonylureas can be employed as active substances in medicaments, in particular as lipoxygenase inhibitors.</abstract><oa>free_for_read</oa></addata></record>
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subjects	CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title	SUBSTITUIERTE (CHINOLIN-2-YL-METHOXY)PHENYL-N,N'-SULFONYLHARNSTOFFE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG IN ARZNEIMITTELN
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