Verfahren zur Herstellung neuer 5-Aryl-, bzw. Heteroaryl-Benzotetrahydrodiazepin-24-dione
1,274,029. Psychosedative &c compositions. BOEHRINGER INGELHEIM G.m.b.H. 14 July, 1969 [12 July, 1968 (2)], No. 35374/69. Heading A5B. [Also in Division C2] Pharmaceutical compositions comprise a compound of the formula: (R 1 =C 1-4 alkyl optionally substituted by halogen, OH, alkoxy, acyloxy, C...
Gespeichert in:
Hauptverfasser: | , , |
---|---|
Format: | Patent |
Sprache: | ger |
Schlagworte: | |
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 | WEBER,KARL-HEINZ,DR MERZ,HERBERT,DR ZEILE,KARL |
description | 1,274,029. Psychosedative &c compositions. BOEHRINGER INGELHEIM G.m.b.H. 14 July, 1969 [12 July, 1968 (2)], No. 35374/69. Heading A5B. [Also in Division C2] Pharmaceutical compositions comprise a compound of the formula: (R 1 =C 1-4 alkyl optionally substituted by halogen, OH, alkoxy, acyloxy, C 2-4 dialkylamino or 5-6 membered N-containing heterocyclic ring linked via the N atom, unsubstituted or mono- or di-methyl or monochloro substituted allyl, cyclohexyl, C 4-7 cycloalkylmethyl or cycloalkenylmethyl, unsubstituted or mono- or di-methyl, -methoxy or -chloro substituted aryl, C 7-8 phenylalkyl, heteroaryl; R 2 =H, Me; R 3 =naphthyl, pyrimidyl, pyrazinyl, pyridazinyl, thienyl, furyl, unsubstituted or methyl or halogen substituted pyridyl or group of the formula: wherein R 5 =H, halogen, Me, Et, MeOCF 3 , CN, NO 2 , C 2-3 acyl or alkoxycarbonyl; R 6 = H, halogen, Me, Et, MeO; R 4 =H, halogen, Me, MeO, CF 3 , CN, C 2-3 acyl or alkoxycarbonyl), with or without other active ingredients (e.g. spasmolytics and/or psychopharmaceuticals), in association with a carrier. The primary active ingredients are psychosedatives and anticonvulsants. Reference has been directed by the Comptroller to Specification 1,210,809; 1,210,810; 1,214,662; 1,214,663 and 1,217,217. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CH517103A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CH517103A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CH517103A3</originalsourceid><addsrcrecordid>eNqFikEKwjAUBbtxIeoVJAcwYm2L61qUHkAEV-VrXm0g_JTfFGlOr4J7VwMzM09uV0hLnYBVHEXVkCHAuZGfijFCVKFLmZzeqHt8bT89QDx9zREcfUAQ6iYj3liK6C3rfa6N9YxlMmvJDVj9uEjW59OlqjV632Do6QFGaKq6SA_pLiuzv8MbUOQ45Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Verfahren zur Herstellung neuer 5-Aryl-, bzw. Heteroaryl-Benzotetrahydrodiazepin-24-dione</title><source>esp@cenet</source><creator>WEBER,KARL-HEINZ,DR ; MERZ,HERBERT,DR ; ZEILE,KARL</creator><creatorcontrib>WEBER,KARL-HEINZ,DR ; MERZ,HERBERT,DR ; ZEILE,KARL</creatorcontrib><description>1,274,029. Psychosedative &c compositions. BOEHRINGER INGELHEIM G.m.b.H. 14 July, 1969 [12 July, 1968 (2)], No. 35374/69. Heading A5B. [Also in Division C2] Pharmaceutical compositions comprise a compound of the formula: (R 1 =C 1-4 alkyl optionally substituted by halogen, OH, alkoxy, acyloxy, C 2-4 dialkylamino or 5-6 membered N-containing heterocyclic ring linked via the N atom, unsubstituted or mono- or di-methyl or monochloro substituted allyl, cyclohexyl, C 4-7 cycloalkylmethyl or cycloalkenylmethyl, unsubstituted or mono- or di-methyl, -methoxy or -chloro substituted aryl, C 7-8 phenylalkyl, heteroaryl; R 2 =H, Me; R 3 =naphthyl, pyrimidyl, pyrazinyl, pyridazinyl, thienyl, furyl, unsubstituted or methyl or halogen substituted pyridyl or group of the formula: wherein R 5 =H, halogen, Me, Et, MeOCF 3 , CN, NO 2 , C 2-3 acyl or alkoxycarbonyl; R 6 = H, halogen, Me, Et, MeO; R 4 =H, halogen, Me, MeO, CF 3 , CN, C 2-3 acyl or alkoxycarbonyl), with or without other active ingredients (e.g. spasmolytics and/or psychopharmaceuticals), in association with a carrier. The primary active ingredients are psychosedatives and anticonvulsants. Reference has been directed by the Comptroller to Specification 1,210,809; 1,210,810; 1,214,662; 1,214,663 and 1,217,217.</description><edition>1</edition><language>ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1971</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=19711231&DB=EPODOC&CC=CH&NR=517103A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19711231&DB=EPODOC&CC=CH&NR=517103A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>WEBER,KARL-HEINZ,DR</creatorcontrib><creatorcontrib>MERZ,HERBERT,DR</creatorcontrib><creatorcontrib>ZEILE,KARL</creatorcontrib><title>Verfahren zur Herstellung neuer 5-Aryl-, bzw. Heteroaryl-Benzotetrahydrodiazepin-24-dione</title><description>1,274,029. Psychosedative &c compositions. BOEHRINGER INGELHEIM G.m.b.H. 14 July, 1969 [12 July, 1968 (2)], No. 35374/69. Heading A5B. [Also in Division C2] Pharmaceutical compositions comprise a compound of the formula: (R 1 =C 1-4 alkyl optionally substituted by halogen, OH, alkoxy, acyloxy, C 2-4 dialkylamino or 5-6 membered N-containing heterocyclic ring linked via the N atom, unsubstituted or mono- or di-methyl or monochloro substituted allyl, cyclohexyl, C 4-7 cycloalkylmethyl or cycloalkenylmethyl, unsubstituted or mono- or di-methyl, -methoxy or -chloro substituted aryl, C 7-8 phenylalkyl, heteroaryl; R 2 =H, Me; R 3 =naphthyl, pyrimidyl, pyrazinyl, pyridazinyl, thienyl, furyl, unsubstituted or methyl or halogen substituted pyridyl or group of the formula: wherein R 5 =H, halogen, Me, Et, MeOCF 3 , CN, NO 2 , C 2-3 acyl or alkoxycarbonyl; R 6 = H, halogen, Me, Et, MeO; R 4 =H, halogen, Me, MeO, CF 3 , CN, C 2-3 acyl or alkoxycarbonyl), with or without other active ingredients (e.g. spasmolytics and/or psychopharmaceuticals), in association with a carrier. The primary active ingredients are psychosedatives and anticonvulsants. Reference has been directed by the Comptroller to Specification 1,210,809; 1,210,810; 1,214,662; 1,214,663 and 1,217,217.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1971</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFikEKwjAUBbtxIeoVJAcwYm2L61qUHkAEV-VrXm0g_JTfFGlOr4J7VwMzM09uV0hLnYBVHEXVkCHAuZGfijFCVKFLmZzeqHt8bT89QDx9zREcfUAQ6iYj3liK6C3rfa6N9YxlMmvJDVj9uEjW59OlqjV632Do6QFGaKq6SA_pLiuzv8MbUOQ45Q</recordid><startdate>19711231</startdate><enddate>19711231</enddate><creator>WEBER,KARL-HEINZ,DR</creator><creator>MERZ,HERBERT,DR</creator><creator>ZEILE,KARL</creator><scope>EVB</scope></search><sort><creationdate>19711231</creationdate><title>Verfahren zur Herstellung neuer 5-Aryl-, bzw. Heteroaryl-Benzotetrahydrodiazepin-24-dione</title><author>WEBER,KARL-HEINZ,DR ; MERZ,HERBERT,DR ; ZEILE,KARL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CH517103A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1971</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>WEBER,KARL-HEINZ,DR</creatorcontrib><creatorcontrib>MERZ,HERBERT,DR</creatorcontrib><creatorcontrib>ZEILE,KARL</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WEBER,KARL-HEINZ,DR</au><au>MERZ,HERBERT,DR</au><au>ZEILE,KARL</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Verfahren zur Herstellung neuer 5-Aryl-, bzw. Heteroaryl-Benzotetrahydrodiazepin-24-dione</title><date>1971-12-31</date><risdate>1971</risdate><abstract>1,274,029. Psychosedative &c compositions. BOEHRINGER INGELHEIM G.m.b.H. 14 July, 1969 [12 July, 1968 (2)], No. 35374/69. Heading A5B. [Also in Division C2] Pharmaceutical compositions comprise a compound of the formula: (R 1 =C 1-4 alkyl optionally substituted by halogen, OH, alkoxy, acyloxy, C 2-4 dialkylamino or 5-6 membered N-containing heterocyclic ring linked via the N atom, unsubstituted or mono- or di-methyl or monochloro substituted allyl, cyclohexyl, C 4-7 cycloalkylmethyl or cycloalkenylmethyl, unsubstituted or mono- or di-methyl, -methoxy or -chloro substituted aryl, C 7-8 phenylalkyl, heteroaryl; R 2 =H, Me; R 3 =naphthyl, pyrimidyl, pyrazinyl, pyridazinyl, thienyl, furyl, unsubstituted or methyl or halogen substituted pyridyl or group of the formula: wherein R 5 =H, halogen, Me, Et, MeOCF 3 , CN, NO 2 , C 2-3 acyl or alkoxycarbonyl; R 6 = H, halogen, Me, Et, MeO; R 4 =H, halogen, Me, MeO, CF 3 , CN, C 2-3 acyl or alkoxycarbonyl), with or without other active ingredients (e.g. spasmolytics and/or psychopharmaceuticals), in association with a carrier. The primary active ingredients are psychosedatives and anticonvulsants. Reference has been directed by the Comptroller to Specification 1,210,809; 1,210,810; 1,214,662; 1,214,663 and 1,217,217.</abstract><edition>1</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | ger |
recordid | cdi_epo_espacenet_CH517103A |
source | esp@cenet |
subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Verfahren zur Herstellung neuer 5-Aryl-, bzw. Heteroaryl-Benzotetrahydrodiazepin-24-dione |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T22%3A04%3A25IST&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=WEBER,KARL-HEINZ,DR&rft.date=1971-12-31&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECH517103A%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 |