Imidazoles
Verbindungen der Formel, worin R1 (H), Halogen, Alkyl, Alkoxy, Alkoxycarbonyl oder Cyan, R2 (H), Alkyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl oder Alkoxycarbonyl, R3 (H), Alkyl, Formyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl, Aminoalkyl, Mono- oder Dialkylaminoalkyl, Nitroso, Nitro, Amino, Mono- oder Dia...
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creator | SCHUDT, CHRISTIAN RAINER, GEORG RIEDEL, RICHARD SCHAEFER, HARTMANN KLEMM, KURT, DR SENN-BILFINGER GRUNDLER, GERHARD SIMON, WOLFGANG |
description | Verbindungen der Formel, worin R1 (H), Halogen, Alkyl, Alkoxy, Alkoxycarbonyl oder Cyan, R2 (H), Alkyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl oder Alkoxycarbonyl, R3 (H), Alkyl, Formyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl, Aminoalkyl, Mono- oder Dialkylaminoalkyl, Nitroso, Nitro, Amino, Mono- oder Dialkylamino oder Alkoxycarbonyl, R4 (H), Alkyl, Alkoxy, Halogen oder Trifluormethyl, R5 (H), Alkyl, Alkoxy, Halogen oder Trifluormethyl, R6 H oder Alkyl, n die Zahlen 1 oder 2, G1 CH oder N G2 O, NH, NAlkyl, S, (=CH-) oder Alkylen, G3 Ethylen, Trimethylen, Tetramethylen, Pentamethylen, Propenylen, 1-Butenylen oder 2-Butylen-G4 S, O oder (-CH=CH-) bedeutet, sind neue Verbindungen mit interessanten pharmakologischen Eigenschaften. Sie weisen insbesondere eine ausgezeichnete Magen- und Darmschutzwirkung bei Warmblütern auf.
Compounds of formula (I), in which R1 is H, halogen, alkyl, alkoxy, alkoxycarbonyl or cyanogen; R2 is H, alkyl, hydroxyalkyl, haloalkyl, cyanoalkyl or alkoxycarbonyl; R3 is H, alkyl, formyl, hydroxyalkyl, haloalkyl, cyanoalkyl, aminoalkyl, mono- or dialkylaminoalkyl, nitroso, nitro, amino, mono- or dialkylamino or alkoxycarbonyl; R4 is H, alkyl, alkoxy, halogen or trifluoromethyl; R5 is H, alkyl, alkoxy, halogen or trifluoromethyl; R6 is H or alkyl; n is 1 or 2; G1 is CH or N; G2 is O, NH, N-alkyl, S, (=CH-) or alkylene; G3 is ethylene, trimethylene, tetramethylene, pentamethylene, propenylene, 1-butenylene or 2-butenylene; G4 is S, O or (-CH=CH-). These compounds have interesting pharmacological properties. They have in particular a protective effect on the stomach and intestines of warm-blooded animals. |
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Compounds of formula (I), in which R1 is H, halogen, alkyl, alkoxy, alkoxycarbonyl or cyanogen; R2 is H, alkyl, hydroxyalkyl, haloalkyl, cyanoalkyl or alkoxycarbonyl; R3 is H, alkyl, formyl, hydroxyalkyl, haloalkyl, cyanoalkyl, aminoalkyl, mono- or dialkylaminoalkyl, nitroso, nitro, amino, mono- or dialkylamino or alkoxycarbonyl; R4 is H, alkyl, alkoxy, halogen or trifluoromethyl; R5 is H, alkyl, alkoxy, halogen or trifluoromethyl; R6 is H or alkyl; n is 1 or 2; G1 is CH or N; G2 is O, NH, N-alkyl, S, (=CH-) or alkylene; G3 is ethylene, trimethylene, tetramethylene, pentamethylene, propenylene, 1-butenylene or 2-butenylene; G4 is S, O or (-CH=CH-). These compounds have interesting pharmacological properties. They have in particular a protective effect on the stomach and intestines of warm-blooded animals.</description><edition>4</edition><language>eng ; fre ; ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1988</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=19881109&DB=EPODOC&CC=EP&NR=0290003A2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19881109&DB=EPODOC&CC=EP&NR=0290003A2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SCHUDT, CHRISTIAN</creatorcontrib><creatorcontrib>RAINER, GEORG</creatorcontrib><creatorcontrib>RIEDEL, RICHARD</creatorcontrib><creatorcontrib>SCHAEFER, HARTMANN</creatorcontrib><creatorcontrib>KLEMM, KURT, DR</creatorcontrib><creatorcontrib>SENN-BILFINGER</creatorcontrib><creatorcontrib>GRUNDLER, GERHARD</creatorcontrib><creatorcontrib>SIMON, WOLFGANG</creatorcontrib><title>Imidazoles</title><description>Verbindungen der Formel, worin R1 (H), Halogen, Alkyl, Alkoxy, Alkoxycarbonyl oder Cyan, R2 (H), Alkyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl oder Alkoxycarbonyl, R3 (H), Alkyl, Formyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl, Aminoalkyl, Mono- oder Dialkylaminoalkyl, Nitroso, Nitro, Amino, Mono- oder Dialkylamino oder Alkoxycarbonyl, R4 (H), Alkyl, Alkoxy, Halogen oder Trifluormethyl, R5 (H), Alkyl, Alkoxy, Halogen oder Trifluormethyl, R6 H oder Alkyl, n die Zahlen 1 oder 2, G1 CH oder N G2 O, NH, NAlkyl, S, (=CH-) oder Alkylen, G3 Ethylen, Trimethylen, Tetramethylen, Pentamethylen, Propenylen, 1-Butenylen oder 2-Butylen-G4 S, O oder (-CH=CH-) bedeutet, sind neue Verbindungen mit interessanten pharmakologischen Eigenschaften. Sie weisen insbesondere eine ausgezeichnete Magen- und Darmschutzwirkung bei Warmblütern auf.
Compounds of formula (I), in which R1 is H, halogen, alkyl, alkoxy, alkoxycarbonyl or cyanogen; R2 is H, alkyl, hydroxyalkyl, haloalkyl, cyanoalkyl or alkoxycarbonyl; R3 is H, alkyl, formyl, hydroxyalkyl, haloalkyl, cyanoalkyl, aminoalkyl, mono- or dialkylaminoalkyl, nitroso, nitro, amino, mono- or dialkylamino or alkoxycarbonyl; R4 is H, alkyl, alkoxy, halogen or trifluoromethyl; R5 is H, alkyl, alkoxy, halogen or trifluoromethyl; R6 is H or alkyl; n is 1 or 2; G1 is CH or N; G2 is O, NH, N-alkyl, S, (=CH-) or alkylene; G3 is ethylene, trimethylene, tetramethylene, pentamethylene, propenylene, 1-butenylene or 2-butenylene; G4 is S, O or (-CH=CH-). These compounds have interesting pharmacological properties. They have in particular a protective effect on the stomach and intestines of warm-blooded animals.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1988</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZODyzM1MSazKz0kt5mFgTUvMKU7lhdLcDApuriHOHrqpBfnxqcUFicmpeakl8a4BBkaWBgYGxo5GxkQoAQCOMByI</recordid><startdate>19881109</startdate><enddate>19881109</enddate><creator>SCHUDT, CHRISTIAN</creator><creator>RAINER, GEORG</creator><creator>RIEDEL, RICHARD</creator><creator>SCHAEFER, HARTMANN</creator><creator>KLEMM, KURT, DR</creator><creator>SENN-BILFINGER</creator><creator>GRUNDLER, GERHARD</creator><creator>SIMON, WOLFGANG</creator><scope>EVB</scope></search><sort><creationdate>19881109</creationdate><title>Imidazoles</title><author>SCHUDT, CHRISTIAN ; RAINER, GEORG ; RIEDEL, RICHARD ; SCHAEFER, HARTMANN ; KLEMM, KURT, DR ; SENN-BILFINGER ; GRUNDLER, GERHARD ; SIMON, WOLFGANG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP0290003A23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>1988</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>SCHUDT, CHRISTIAN</creatorcontrib><creatorcontrib>RAINER, GEORG</creatorcontrib><creatorcontrib>RIEDEL, RICHARD</creatorcontrib><creatorcontrib>SCHAEFER, HARTMANN</creatorcontrib><creatorcontrib>KLEMM, KURT, DR</creatorcontrib><creatorcontrib>SENN-BILFINGER</creatorcontrib><creatorcontrib>GRUNDLER, GERHARD</creatorcontrib><creatorcontrib>SIMON, WOLFGANG</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SCHUDT, CHRISTIAN</au><au>RAINER, GEORG</au><au>RIEDEL, RICHARD</au><au>SCHAEFER, HARTMANN</au><au>KLEMM, KURT, DR</au><au>SENN-BILFINGER</au><au>GRUNDLER, GERHARD</au><au>SIMON, WOLFGANG</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Imidazoles</title><date>1988-11-09</date><risdate>1988</risdate><abstract>Verbindungen der Formel, worin R1 (H), Halogen, Alkyl, Alkoxy, Alkoxycarbonyl oder Cyan, R2 (H), Alkyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl oder Alkoxycarbonyl, R3 (H), Alkyl, Formyl, Hydroxyalkyl, Haloalkyl, Cyanoalkyl, Aminoalkyl, Mono- oder Dialkylaminoalkyl, Nitroso, Nitro, Amino, Mono- oder Dialkylamino oder Alkoxycarbonyl, R4 (H), Alkyl, Alkoxy, Halogen oder Trifluormethyl, R5 (H), Alkyl, Alkoxy, Halogen oder Trifluormethyl, R6 H oder Alkyl, n die Zahlen 1 oder 2, G1 CH oder N G2 O, NH, NAlkyl, S, (=CH-) oder Alkylen, G3 Ethylen, Trimethylen, Tetramethylen, Pentamethylen, Propenylen, 1-Butenylen oder 2-Butylen-G4 S, O oder (-CH=CH-) bedeutet, sind neue Verbindungen mit interessanten pharmakologischen Eigenschaften. Sie weisen insbesondere eine ausgezeichnete Magen- und Darmschutzwirkung bei Warmblütern auf.
Compounds of formula (I), in which R1 is H, halogen, alkyl, alkoxy, alkoxycarbonyl or cyanogen; R2 is H, alkyl, hydroxyalkyl, haloalkyl, cyanoalkyl or alkoxycarbonyl; R3 is H, alkyl, formyl, hydroxyalkyl, haloalkyl, cyanoalkyl, aminoalkyl, mono- or dialkylaminoalkyl, nitroso, nitro, amino, mono- or dialkylamino or alkoxycarbonyl; R4 is H, alkyl, alkoxy, halogen or trifluoromethyl; R5 is H, alkyl, alkoxy, halogen or trifluoromethyl; R6 is H or alkyl; n is 1 or 2; G1 is CH or N; G2 is O, NH, N-alkyl, S, (=CH-) or alkylene; G3 is ethylene, trimethylene, tetramethylene, pentamethylene, propenylene, 1-butenylene or 2-butenylene; G4 is S, O or (-CH=CH-). These compounds have interesting pharmacological properties. They have in particular a protective effect on the stomach and intestines of warm-blooded animals.</abstract><edition>4</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Imidazoles |
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