2-SUBSTITUTED 1,2,3,4,6,7,12,12A-OCTAHYDROPYRAZINO %2@,1@.6,1PYRIDO%3,4-B<INDOLES
Pharmacologically active 2-substituted-1,2,3,4,-6,7,12,12A-octahydropyrazino[2',1':6,1]pyrido[3 ,4-b]indoles corresponding to the formula WHEREIN X is a straight or branched chain alkylene group optionally interrupted by a CO or a CHOH group, R is hydrogen, lower alkyl, aryl, aryloxy, cyan...
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creator | ANIL KUMAR SAXENA BHOLA NATH DHAWAN PRITHVI RAJ DUA NITYA ANAND RIKHAB CHAND SRIMAL GURBAKHSH SINGH PADAM CHAND JAIN |
description | Pharmacologically active 2-substituted-1,2,3,4,-6,7,12,12A-octahydropyrazino[2',1':6,1]pyrido[3 ,4-b]indoles corresponding to the formula WHEREIN X is a straight or branched chain alkylene group optionally interrupted by a CO or a CHOH group, R is hydrogen, lower alkyl, aryl, aryloxy, cyano, carboxy, carbalkoxy, dialkylamino, benzodioxanyl or 4-pyridyl, and X and R together may be hydrogen; Y and Z independently are H2 or an oxygen atom; and R' is hydrogen or a lower alkyl group. The compounds of the invention have tranquilizing and hypotensive activity. The inventive compounds are prepared by reacting an alkyl 1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate starting material with ethyleneimine to give a 1-oxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]-pyrido[3,4-b]indole in which substituents are then introduced at position 2 by a variety of methods, before or after having hydrogenated the oxo group at position 1. Alternatively, an alkyl 2-chloro-acetyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate and a primary amine H2NXR are reacted to give a 1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]pyrido[3,4-b] indole, in which substituents are then introduced before or after having hydrogenated the two oxo groups at positions 1 and 4. |
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The compounds of the invention have tranquilizing and hypotensive activity. The inventive compounds are prepared by reacting an alkyl 1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate starting material with ethyleneimine to give a 1-oxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]-pyrido[3,4-b]indole in which substituents are then introduced at position 2 by a variety of methods, before or after having hydrogenated the oxo group at position 1. Alternatively, an alkyl 2-chloro-acetyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate and a primary amine H2NXR are reacted to give a 1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]pyrido[3,4-b] indole, in which substituents are then introduced before or after having hydrogenated the two oxo groups at positions 1 and 4.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1975</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=19750424&DB=EPODOC&CC=AU&NR=6164973A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76516</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19750424&DB=EPODOC&CC=AU&NR=6164973A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>ANIL KUMAR SAXENA</creatorcontrib><creatorcontrib>BHOLA NATH DHAWAN</creatorcontrib><creatorcontrib>PRITHVI RAJ DUA</creatorcontrib><creatorcontrib>NITYA ANAND</creatorcontrib><creatorcontrib>RIKHAB CHAND SRIMAL</creatorcontrib><creatorcontrib>GURBAKHSH SINGH</creatorcontrib><creatorcontrib>PADAM CHAND JAIN</creatorcontrib><title>2-SUBSTITUTED 1,2,3,4,6,7,12,12A-OCTAHYDROPYRAZINO %2@,1@.6,1PYRIDO%3,4-B<INDOLES</title><description>Pharmacologically active 2-substituted-1,2,3,4,-6,7,12,12A-octahydropyrazino[2',1':6,1]pyrido[3 ,4-b]indoles corresponding to the formula WHEREIN X is a straight or branched chain alkylene group optionally interrupted by a CO or a CHOH group, R is hydrogen, lower alkyl, aryl, aryloxy, cyano, carboxy, carbalkoxy, dialkylamino, benzodioxanyl or 4-pyridyl, and X and R together may be hydrogen; Y and Z independently are H2 or an oxygen atom; and R' is hydrogen or a lower alkyl group. The compounds of the invention have tranquilizing and hypotensive activity. The inventive compounds are prepared by reacting an alkyl 1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate starting material with ethyleneimine to give a 1-oxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]-pyrido[3,4-b]indole in which substituents are then introduced at position 2 by a variety of methods, before or after having hydrogenated the oxo group at position 1. Alternatively, an alkyl 2-chloro-acetyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate and a primary amine H2NXR are reacted to give a 1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]pyrido[3,4-b] indole, in which substituents are then introduced before or after having hydrogenated the two oxo groups at positions 1 and 4.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1975</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZAg00g0OdQoO8QwJDXF1UTDUMdIx1jHRMdMx1zE0AiJHXX_nEEePSJcg_4DIIMcoTz9_BVUjBx1DBz0zHUOgkKeLvypQh66Tjaefi7-PazAPA2taYk5xKi-U5maQd3MNcfbQTS3Ij08tLkhMTs1LLYl3DDUzNDOxNDd2NCasAgDjUyyK</recordid><startdate>19750424</startdate><enddate>19750424</enddate><creator>ANIL KUMAR SAXENA</creator><creator>BHOLA NATH DHAWAN</creator><creator>PRITHVI RAJ DUA</creator><creator>NITYA ANAND</creator><creator>RIKHAB CHAND SRIMAL</creator><creator>GURBAKHSH SINGH</creator><creator>PADAM CHAND JAIN</creator><scope>EVB</scope></search><sort><creationdate>19750424</creationdate><title>2-SUBSTITUTED 1,2,3,4,6,7,12,12A-OCTAHYDROPYRAZINO %2@,1@.6,1PYRIDO%3,4-B<INDOLES</title><author>ANIL KUMAR SAXENA ; BHOLA NATH DHAWAN ; PRITHVI RAJ DUA ; NITYA ANAND ; RIKHAB CHAND SRIMAL ; GURBAKHSH SINGH ; PADAM CHAND JAIN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_AU6164973A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1975</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>ANIL KUMAR SAXENA</creatorcontrib><creatorcontrib>BHOLA NATH DHAWAN</creatorcontrib><creatorcontrib>PRITHVI RAJ DUA</creatorcontrib><creatorcontrib>NITYA ANAND</creatorcontrib><creatorcontrib>RIKHAB CHAND SRIMAL</creatorcontrib><creatorcontrib>GURBAKHSH SINGH</creatorcontrib><creatorcontrib>PADAM CHAND JAIN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>ANIL KUMAR SAXENA</au><au>BHOLA NATH DHAWAN</au><au>PRITHVI RAJ DUA</au><au>NITYA ANAND</au><au>RIKHAB CHAND SRIMAL</au><au>GURBAKHSH SINGH</au><au>PADAM CHAND JAIN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>2-SUBSTITUTED 1,2,3,4,6,7,12,12A-OCTAHYDROPYRAZINO %2@,1@.6,1PYRIDO%3,4-B<INDOLES</title><date>1975-04-24</date><risdate>1975</risdate><abstract>Pharmacologically active 2-substituted-1,2,3,4,-6,7,12,12A-octahydropyrazino[2',1':6,1]pyrido[3 ,4-b]indoles corresponding to the formula WHEREIN X is a straight or branched chain alkylene group optionally interrupted by a CO or a CHOH group, R is hydrogen, lower alkyl, aryl, aryloxy, cyano, carboxy, carbalkoxy, dialkylamino, benzodioxanyl or 4-pyridyl, and X and R together may be hydrogen; Y and Z independently are H2 or an oxygen atom; and R' is hydrogen or a lower alkyl group. The compounds of the invention have tranquilizing and hypotensive activity. The inventive compounds are prepared by reacting an alkyl 1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate starting material with ethyleneimine to give a 1-oxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]-pyrido[3,4-b]indole in which substituents are then introduced at position 2 by a variety of methods, before or after having hydrogenated the oxo group at position 1. Alternatively, an alkyl 2-chloro-acetyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylate and a primary amine H2NXR are reacted to give a 1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino[2',1':6,1]pyrido[3,4-b] indole, in which substituents are then introduced before or after having hydrogenated the two oxo groups at positions 1 and 4.</abstract><oa>free_for_read</oa></addata></record> |
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title | 2-SUBSTITUTED 1,2,3,4,6,7,12,12A-OCTAHYDROPYRAZINO %2@,1@.6,1PYRIDO%3,4-B<INDOLES |
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