Verfahren zur Herstellung von Oxazaheterocyclen

(A) Dibenzo (b,f) (1,4) oxazepines Am=an amino group; A=an alkylene residue separating Am and N by at least 2 C atoms. X =O or H2 and at least one of A and B is substd. by NO2, and may be further substd. by alkyl, O-alkyl, CF3, NH2 or halogen. (B) Salts of (I) (C) Intermediates (III) (III) Intermedi...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
1. Verfasser:	NAGARAJAN,KUPPUSWAMY,DR
Format:	Patent
Sprache:	ger
Schlagworte:	CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
Online-Zugang:	Volltext bestellen
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

container_end_page
container_issue
container_start_page
container_title
container_volume
creator	NAGARAJAN,KUPPUSWAMY,DR
description	(A) Dibenzo (b,f) (1,4) oxazepines Am=an amino group; A=an alkylene residue separating Am and N by at least 2 C atoms. X =O or H2 and at least one of A and B is substd. by NO2, and may be further substd. by alkyl, O-alkyl, CF3, NH2 or halogen. (B) Salts of (I) (C) Intermediates (III) (III) Intermediates for (I) and (II) (I) and (II) - Antidepressants, with anti-acetylcholine, anti-serotonin, antihistamine, antiphlogistic, and local anaesthetic activity. Dose 0.05-0.2 g/day.
format	Patent
fullrecord	<record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CH484180A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CH484180A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CH484180A3</originalsourceid><addsrcrecordid>eNrjZNAPSy1KS8woSs1TqCotUvBILSouSc3JKc1LVyjLz1Pwr0isSsxILUktyk-uTM5JzeNhYE1LzClO5YXS3Axybq4hzh66qQX58anFBYnJqXmpJfHOHiYWJoYWBo7GBBUAAG-PKkA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Verfahren zur Herstellung von Oxazaheterocyclen</title><source>esp@cenet</source><creator>NAGARAJAN,KUPPUSWAMY,DR</creator><creatorcontrib>NAGARAJAN,KUPPUSWAMY,DR</creatorcontrib><description>(A) Dibenzo (b,f) (1,4) oxazepines Am=an amino group; A=an alkylene residue separating Am and N by at least 2 C atoms. X =O or H2 and at least one of A and B is substd. by NO2, and may be further substd. by alkyl, O-alkyl, CF3, NH2 or halogen. (B) Salts of (I) (C) Intermediates (III) (III) Intermediates for (I) and (II) (I) and (II) - Antidepressants, with anti-acetylcholine, anti-serotonin, antihistamine, antiphlogistic, and local anaesthetic activity. Dose 0.05-0.2 g/day.</description><edition>1</edition><language>ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>1970</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=19700115&DB=EPODOC&CC=CH&NR=484180A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19700115&DB=EPODOC&CC=CH&NR=484180A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAGARAJAN,KUPPUSWAMY,DR</creatorcontrib><title>Verfahren zur Herstellung von Oxazaheterocyclen</title><description>(A) Dibenzo (b,f) (1,4) oxazepines Am=an amino group; A=an alkylene residue separating Am and N by at least 2 C atoms. X =O or H2 and at least one of A and B is substd. by NO2, and may be further substd. by alkyl, O-alkyl, CF3, NH2 or halogen. (B) Salts of (I) (C) Intermediates (III) (III) Intermediates for (I) and (II) (I) and (II) - Antidepressants, with anti-acetylcholine, anti-serotonin, antihistamine, antiphlogistic, and local anaesthetic activity. Dose 0.05-0.2 g/day.</description><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><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1970</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNAPSy1KS8woSs1TqCotUvBILSouSc3JKc1LVyjLz1Pwr0isSsxILUktyk-uTM5JzeNhYE1LzClO5YXS3Axybq4hzh66qQX58anFBYnJqXmpJfHOHiYWJoYWBo7GBBUAAG-PKkA</recordid><startdate>19700115</startdate><enddate>19700115</enddate><creator>NAGARAJAN,KUPPUSWAMY,DR</creator><scope>EVB</scope></search><sort><creationdate>19700115</creationdate><title>Verfahren zur Herstellung von Oxazaheterocyclen</title><author>NAGARAJAN,KUPPUSWAMY,DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CH484180A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1970</creationdate><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><toplevel>online_resources</toplevel><creatorcontrib>NAGARAJAN,KUPPUSWAMY,DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAGARAJAN,KUPPUSWAMY,DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Verfahren zur Herstellung von Oxazaheterocyclen</title><date>1970-01-15</date><risdate>1970</risdate><abstract>(A) Dibenzo (b,f) (1,4) oxazepines Am=an amino group; A=an alkylene residue separating Am and N by at least 2 C atoms. X =O or H2 and at least one of A and B is substd. by NO2, and may be further substd. by alkyl, O-alkyl, CF3, NH2 or halogen. (B) Salts of (I) (C) Intermediates (III) (III) Intermediates for (I) and (II) (I) and (II) - Antidepressants, with anti-acetylcholine, anti-serotonin, antihistamine, antiphlogistic, and local anaesthetic activity. Dose 0.05-0.2 g/day.</abstract><edition>1</edition><oa>free_for_read</oa></addata></record>
fulltext	fulltext_linktorsrc
identifier
ispartof
issn
language	ger
recordid	cdi_epo_espacenet_CH484180A
source	esp@cenet
subjects	CHEMISTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
title	Verfahren zur Herstellung von Oxazaheterocyclen
url	https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T00%3A00%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=NAGARAJAN,KUPPUSWAMY,DR&rft.date=1970-01-15&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECH484180A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true