7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and preparation method thereof
The invention discloses 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and a preparation method thereof. The method comprises the following steps: taking 3,4-dimethoxyhydrocinnamic acid as a starting material, catalyzing by thionyl chloride and then carrying out aminolysis treatme...
Gespeichert in:
Hauptverfasser: | , , , , , |
---|---|
Format: | Patent |
Sprache: | chi ; eng |
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 | JIN QINGXIAN CHEN SHUYU QIAO WENJUN ZHANG HONGPEI FANG SHAOMING ZHEN YAOYAO |
description | The invention discloses 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and a preparation method thereof. The method comprises the following steps: taking 3,4-dimethoxyhydrocinnamic acid as a starting material, catalyzing by thionyl chloride and then carrying out aminolysis treatment to obtain 3,4-dimethoxyphenyl propanamide; carrying out reductive treatment by boron trifluoride diethyl etherate and sodium borohydride to obtain 3,4-dimethoxy-amphetamine; carrying out reaction on the 3,4-dimethoxy-amphetamine in sulfuric acid and paraformaldehyde to obtain N-acetyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine after acetyl protection; carrying out acetyl deprotection and Boc deprotection to obtain N-Boc-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine; introducing hydrochloric acid gas to obtain the 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride. The preparation method is relative mild in conditions, and a product is easy to process and purify, and is suitable for |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN107298655A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN107298655A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN107298655A3</originalsourceid><addsrcrecordid>eNqNjLEOgjAYBlkcjPoOdW8TASs4GqJhcnIzBn_pR9oE26Z0EJ7ehPgATjfc5ZbJs-ClUOaNqN1nFBnP-Z5LERED6VEFJ9JavGAnd28fNMEbCzaLVvcuGAVGVjEf4ClQNM6y-aVY1Ahw3TpZdNQP2Py4SraX862qBbxrMHhqYRGb6pruiuxYHqQ85f80X98wPEA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and preparation method thereof</title><source>esp@cenet</source><creator>JIN QINGXIAN ; CHEN SHUYU ; QIAO WENJUN ; ZHANG HONGPEI ; FANG SHAOMING ; ZHEN YAOYAO</creator><creatorcontrib>JIN QINGXIAN ; CHEN SHUYU ; QIAO WENJUN ; ZHANG HONGPEI ; FANG SHAOMING ; ZHEN YAOYAO</creatorcontrib><description>The invention discloses 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and a preparation method thereof. The method comprises the following steps: taking 3,4-dimethoxyhydrocinnamic acid as a starting material, catalyzing by thionyl chloride and then carrying out aminolysis treatment to obtain 3,4-dimethoxyphenyl propanamide; carrying out reductive treatment by boron trifluoride diethyl etherate and sodium borohydride to obtain 3,4-dimethoxy-amphetamine; carrying out reaction on the 3,4-dimethoxy-amphetamine in sulfuric acid and paraformaldehyde to obtain N-acetyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine after acetyl protection; carrying out acetyl deprotection and Boc deprotection to obtain N-Boc-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine; introducing hydrochloric acid gas to obtain the 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride. The preparation method is relative mild in conditions, and a product is easy to process and purify, and is suitable for</description><language>chi ; eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2017</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=20171027&DB=EPODOC&CC=CN&NR=107298655A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20171027&DB=EPODOC&CC=CN&NR=107298655A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JIN QINGXIAN</creatorcontrib><creatorcontrib>CHEN SHUYU</creatorcontrib><creatorcontrib>QIAO WENJUN</creatorcontrib><creatorcontrib>ZHANG HONGPEI</creatorcontrib><creatorcontrib>FANG SHAOMING</creatorcontrib><creatorcontrib>ZHEN YAOYAO</creatorcontrib><title>7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and preparation method thereof</title><description>The invention discloses 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and a preparation method thereof. The method comprises the following steps: taking 3,4-dimethoxyhydrocinnamic acid as a starting material, catalyzing by thionyl chloride and then carrying out aminolysis treatment to obtain 3,4-dimethoxyphenyl propanamide; carrying out reductive treatment by boron trifluoride diethyl etherate and sodium borohydride to obtain 3,4-dimethoxy-amphetamine; carrying out reaction on the 3,4-dimethoxy-amphetamine in sulfuric acid and paraformaldehyde to obtain N-acetyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine after acetyl protection; carrying out acetyl deprotection and Boc deprotection to obtain N-Boc-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine; introducing hydrochloric acid gas to obtain the 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride. The preparation method is relative mild in conditions, and a product is easy to process and purify, and is suitable for</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2017</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjLEOgjAYBlkcjPoOdW8TASs4GqJhcnIzBn_pR9oE26Z0EJ7ehPgATjfc5ZbJs-ClUOaNqN1nFBnP-Z5LERED6VEFJ9JavGAnd28fNMEbCzaLVvcuGAVGVjEf4ClQNM6y-aVY1Ahw3TpZdNQP2Py4SraX862qBbxrMHhqYRGb6pruiuxYHqQ85f80X98wPEA</recordid><startdate>20171027</startdate><enddate>20171027</enddate><creator>JIN QINGXIAN</creator><creator>CHEN SHUYU</creator><creator>QIAO WENJUN</creator><creator>ZHANG HONGPEI</creator><creator>FANG SHAOMING</creator><creator>ZHEN YAOYAO</creator><scope>EVB</scope></search><sort><creationdate>20171027</creationdate><title>7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and preparation method thereof</title><author>JIN QINGXIAN ; CHEN SHUYU ; QIAO WENJUN ; ZHANG HONGPEI ; FANG SHAOMING ; ZHEN YAOYAO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN107298655A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2017</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>JIN QINGXIAN</creatorcontrib><creatorcontrib>CHEN SHUYU</creatorcontrib><creatorcontrib>QIAO WENJUN</creatorcontrib><creatorcontrib>ZHANG HONGPEI</creatorcontrib><creatorcontrib>FANG SHAOMING</creatorcontrib><creatorcontrib>ZHEN YAOYAO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JIN QINGXIAN</au><au>CHEN SHUYU</au><au>QIAO WENJUN</au><au>ZHANG HONGPEI</au><au>FANG SHAOMING</au><au>ZHEN YAOYAO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and preparation method thereof</title><date>2017-10-27</date><risdate>2017</risdate><abstract>The invention discloses 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and a preparation method thereof. The method comprises the following steps: taking 3,4-dimethoxyhydrocinnamic acid as a starting material, catalyzing by thionyl chloride and then carrying out aminolysis treatment to obtain 3,4-dimethoxyphenyl propanamide; carrying out reductive treatment by boron trifluoride diethyl etherate and sodium borohydride to obtain 3,4-dimethoxy-amphetamine; carrying out reaction on the 3,4-dimethoxy-amphetamine in sulfuric acid and paraformaldehyde to obtain N-acetyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine after acetyl protection; carrying out acetyl deprotection and Boc deprotection to obtain N-Boc-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine; introducing hydrochloric acid gas to obtain the 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride. The preparation method is relative mild in conditions, and a product is easy to process and purify, and is suitable for</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | chi ; eng |
recordid | cdi_epo_espacenet_CN107298655A |
source | esp@cenet |
subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine hydrochloride and preparation method thereof |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T07%3A37%3A37IST&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=JIN%20QINGXIAN&rft.date=2017-10-27&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN107298655A%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 |