PROCESS FOR PRODUCING NEW ANTIALLERGIC AND ANTITHROMBOTICHETEROCYCLIC COMPOUNDS
Heterocycles of formula (I) and their pharmaceutically acceptable salts are new, Z = N W =CHR2 when n = 0 or CR2 or CHR2 when n = 1; Y = CH2O, OCH2, CH2S, SCH2, CH2N(R2), N(R2)CH2, CON(R2) or N(R2)CO; n = 0 or 1; R1 = H, lower alkyl, lower alkoxy, lower alkanoyl, halo, CF3, NO2 or CN; R2 = H or lowe...
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| creator | MUSSER,JOHN H.,US KREFT,ANTHONY F.,US KUBRAK,DENNIS M.,US |
| description | Heterocycles of formula (I) and their pharmaceutically acceptable salts are new, Z = N W =CHR2 when n = 0 or CR2 or CHR2 when n = 1; Y = CH2O, OCH2, CH2S, SCH2, CH2N(R2), N(R2)CH2, CON(R2) or N(R2)CO; n = 0 or 1; R1 = H, lower alkyl, lower alkoxy, lower alkanoyl, halo, CF3, NO2 or CN; R2 = H or lower alkyl; R3 = lower alkyl, lower perfluoroalkyl or perfluorophenyl, halo = F, Cl or Br; lower alkyl or alkoxy = 1-6C; lower alkanoyl = 2-6C. Specifically claimed are 3 cpds. (I) viz. N-(3-((2-quinolyl) methoxy)phenyl)ethane sulphonamide, N-(3-((2-quinolyl) methoxy) phenyl) -1-butanesulphonamide and N-(3-((2-quinolyl) methoxy) phenyl) trifluoromethane sulphonamide (Ia). |
| format | Patent |
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Specifically claimed are 3 cpds. (I) viz. N-(3-((2-quinolyl) methoxy)phenyl)ethane sulphonamide, N-(3-((2-quinolyl) methoxy) phenyl) -1-butanesulphonamide and N-(3-((2-quinolyl) methoxy) phenyl) trifluoromethane sulphonamide (Ia).</description><edition>4</edition><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; 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>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=19880328&DB=EPODOC&CC=HU&NR=T44511A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19880328&DB=EPODOC&CC=HU&NR=T44511A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MUSSER,JOHN H.,US</creatorcontrib><creatorcontrib>KREFT,ANTHONY F.,US</creatorcontrib><creatorcontrib>KUBRAK,DENNIS M.,US</creatorcontrib><title>PROCESS FOR PRODUCING NEW ANTIALLERGIC AND ANTITHROMBOTICHETEROCYCLIC COMPOUNDS</title><description>Heterocycles of formula (I) and their pharmaceutically acceptable salts are new, Z = N W =CHR2 when n = 0 or CR2 or CHR2 when n = 1; Y = CH2O, OCH2, CH2S, SCH2, CH2N(R2), N(R2)CH2, CON(R2) or N(R2)CO; n = 0 or 1; R1 = H, lower alkyl, lower alkoxy, lower alkanoyl, halo, CF3, NO2 or CN; R2 = H or lower alkyl; R3 = lower alkyl, lower perfluoroalkyl or perfluorophenyl, halo = F, Cl or Br; lower alkyl or alkoxy = 1-6C; lower alkanoyl = 2-6C. Specifically claimed are 3 cpds. (I) viz. N-(3-((2-quinolyl) methoxy)phenyl)ethane sulphonamide, N-(3-((2-quinolyl) methoxy) phenyl) -1-butanesulphonamide and N-(3-((2-quinolyl) methoxy) phenyl) trifluoromethane sulphonamide (Ia).</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><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><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1988</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPAPCPJ3dg0OVnDzD1IAsl1CnT393BX8XMMVHP1CPB19fFyD3D2dgRwXsECIR5C_r5N_iKezh2uIK1BvpLMPUNrZ3zfAP9TPJZiHgTUtMac4lRdKczPIubmGOHvophbkx6cWFyQmp-allsR7hIaYmJgaGjoaE1QAAHp1Lmg</recordid><startdate>19880328</startdate><enddate>19880328</enddate><creator>MUSSER,JOHN H.,US</creator><creator>KREFT,ANTHONY F.,US</creator><creator>KUBRAK,DENNIS M.,US</creator><scope>EVB</scope></search><sort><creationdate>19880328</creationdate><title>PROCESS FOR PRODUCING NEW ANTIALLERGIC AND ANTITHROMBOTICHETEROCYCLIC COMPOUNDS</title><author>MUSSER,JOHN H.,US ; KREFT,ANTHONY F.,US ; KUBRAK,DENNIS M.,US</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_HUT44511A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1988</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><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><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>MUSSER,JOHN H.,US</creatorcontrib><creatorcontrib>KREFT,ANTHONY F.,US</creatorcontrib><creatorcontrib>KUBRAK,DENNIS M.,US</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MUSSER,JOHN H.,US</au><au>KREFT,ANTHONY F.,US</au><au>KUBRAK,DENNIS M.,US</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCESS FOR PRODUCING NEW ANTIALLERGIC AND ANTITHROMBOTICHETEROCYCLIC COMPOUNDS</title><date>1988-03-28</date><risdate>1988</risdate><abstract>Heterocycles of formula (I) and their pharmaceutically acceptable salts are new, Z = N W =CHR2 when n = 0 or CR2 or CHR2 when n = 1; Y = CH2O, OCH2, CH2S, SCH2, CH2N(R2), N(R2)CH2, CON(R2) or N(R2)CO; n = 0 or 1; R1 = H, lower alkyl, lower alkoxy, lower alkanoyl, halo, CF3, NO2 or CN; R2 = H or lower alkyl; R3 = lower alkyl, lower perfluoroalkyl or perfluorophenyl, halo = F, Cl or Br; lower alkyl or alkoxy = 1-6C; lower alkanoyl = 2-6C. Specifically claimed are 3 cpds. (I) viz. N-(3-((2-quinolyl) methoxy)phenyl)ethane sulphonamide, N-(3-((2-quinolyl) methoxy) phenyl) -1-butanesulphonamide and N-(3-((2-quinolyl) methoxy) phenyl) trifluoromethane sulphonamide (Ia).</abstract><edition>4</edition><oa>free_for_read</oa></addata></record> |
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| subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS 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 | PROCESS FOR PRODUCING NEW ANTIALLERGIC AND ANTITHROMBOTICHETEROCYCLIC COMPOUNDS |
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