PROCESS FOR PREPARING 1,4-DIHYDRO-PYRIDINA DERIVATIVES
Compounds of the formula:where R is an optionally substituted aryl or heteroaryl group;R1 and R are each independently C1-C4 alkyl or 2-methoxyethyl; and Y is -(CH2)n- where n is 2, 3 or 4, -CH2CH(CH3)-or -CH2C(CH3)2-; and their pharmaceutically acceptable salts.The compounds have utility as anti-is...
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creator | CROSS,PETER E.,GB ALKER,DAVID,GB CAMPBELL,SIMON F.,GB |
description | Compounds of the formula:where R is an optionally substituted aryl or heteroaryl group;R1 and R are each independently C1-C4 alkyl or 2-methoxyethyl; and Y is -(CH2)n- where n is 2, 3 or 4, -CH2CH(CH3)-or -CH2C(CH3)2-; and their pharmaceutically acceptable salts.The compounds have utility as anti-ischaemic and antihypertensive agents and as synthetic intermediates to other dihydropyridine calcium antagonists. |
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and Y is -(CH2)n- where n is 2, 3 or 4, -CH2CH(CH3)-or -CH2C(CH3)2-; and their pharmaceutically acceptable salts.The compounds have utility as anti-ischaemic and antihypertensive agents and as synthetic intermediates to other dihydropyridine calcium antagonists.</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=19880128&DB=EPODOC&CC=HU&NR=194172B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19880128&DB=EPODOC&CC=HU&NR=194172B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CROSS,PETER E.,GB</creatorcontrib><creatorcontrib>ALKER,DAVID,GB</creatorcontrib><creatorcontrib>CAMPBELL,SIMON F.,GB</creatorcontrib><title>PROCESS FOR PREPARING 1,4-DIHYDRO-PYRIDINA DERIVATIVES</title><description>Compounds of the formula:where R is an optionally substituted aryl or heteroaryl group;R1 and R are each independently C1-C4 alkyl or 2-methoxyethyl; and Y is -(CH2)n- where n is 2, 3 or 4, -CH2CH(CH3)-or -CH2C(CH3)2-; and their pharmaceutically acceptable salts.The compounds have utility as anti-ischaemic and antihypertensive agents and as synthetic intermediates to other dihydropyridine calcium antagonists.</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>eNrjZDALCPJ3dg0OVnDzD1IICHINcAzy9HNXMNQx0XXx9Ih0CfLXDYgM8nTx9HNUcHEN8gxzDPEMcw3mYWBNS8wpTuWF0twMcm6uIc4euqkF-fGpxQWJyal5qSXxHqGGliaG5kZOxgQVAAAyACbT</recordid><startdate>19880128</startdate><enddate>19880128</enddate><creator>CROSS,PETER E.,GB</creator><creator>ALKER,DAVID,GB</creator><creator>CAMPBELL,SIMON F.,GB</creator><scope>EVB</scope></search><sort><creationdate>19880128</creationdate><title>PROCESS FOR PREPARING 1,4-DIHYDRO-PYRIDINA DERIVATIVES</title><author>CROSS,PETER E.,GB ; 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and Y is -(CH2)n- where n is 2, 3 or 4, -CH2CH(CH3)-or -CH2C(CH3)2-; and their pharmaceutically acceptable salts.The compounds have utility as anti-ischaemic and antihypertensive agents and as synthetic intermediates to other dihydropyridine calcium antagonists.</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 PREPARING 1,4-DIHYDRO-PYRIDINA DERIVATIVES |
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