Preparation method of gadotetrol
The invention provides a gadotetrol preparation process, which comprises the following steps: adding pure water into a gadotetrol crude product for dissolving, performing intermittent ultrasonic treatment by using a digital ultrasonic instrument, introducing inert gas while performing ultrasonic ope...
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creator | WU ZUTI ZHOU SHENGJUN ZHU YIFAN WANG YUXING LU CUIJUN WANG YINGHUI FAN MINHUA NIE LIANGDENG |
description | The invention provides a gadotetrol preparation process, which comprises the following steps: adding pure water into a gadotetrol crude product for dissolving, performing intermittent ultrasonic treatment by using a digital ultrasonic instrument, introducing inert gas while performing ultrasonic operation, slowly dropwise adding ethanol and/or isopropanol during the intermittent period, stopping ultrasonic treatment, continuing magnetic stirring for 1-2 hours, standing for devitrification, filtering, and monitoring the conductivity of filtrate, thereby obtaining the gadotetrol. And finally, freeze-drying to obtain a product with higher purity, improved relaxation rate and reduced renal toxicity.
本发明提供了一种钆特醇制备工艺,将钆特醇粗品加纯水溶解,使用数字超声仪进行间歇超声,超声操作的同时通入惰性气体,间歇期间缓慢滴加乙醇和/或异丙醇,停止超声后继续磁力搅拌1-2h,静置析晶,过滤并监测滤液电导率,最后通过冷冻干燥获得纯度较高弛豫率提高且肾毒性降低的产品。 |
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本发明提供了一种钆特醇制备工艺,将钆特醇粗品加纯水溶解,使用数字超声仪进行间歇超声,超声操作的同时通入惰性气体,间歇期间缓慢滴加乙醇和/或异丙醇,停止超声后继续磁力搅拌1-2h,静置析晶,过滤并监测滤液电导率,最后通过冷冻干燥获得纯度较高弛豫率提高且肾毒性降低的产品。</description><language>chi ; eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2022</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=20220301&DB=EPODOC&CC=CN&NR=114105897A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20220301&DB=EPODOC&CC=CN&NR=114105897A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>WU ZUTI</creatorcontrib><creatorcontrib>ZHOU SHENGJUN</creatorcontrib><creatorcontrib>ZHU YIFAN</creatorcontrib><creatorcontrib>WANG YUXING</creatorcontrib><creatorcontrib>LU CUIJUN</creatorcontrib><creatorcontrib>WANG YINGHUI</creatorcontrib><creatorcontrib>FAN MINHUA</creatorcontrib><creatorcontrib>NIE LIANGDENG</creatorcontrib><title>Preparation method of gadotetrol</title><description>The invention provides a gadotetrol preparation process, which comprises the following steps: adding pure water into a gadotetrol crude product for dissolving, performing intermittent ultrasonic treatment by using a digital ultrasonic instrument, introducing inert gas while performing ultrasonic operation, slowly dropwise adding ethanol and/or isopropanol during the intermittent period, stopping ultrasonic treatment, continuing magnetic stirring for 1-2 hours, standing for devitrification, filtering, and monitoring the conductivity of filtrate, thereby obtaining the gadotetrol. And finally, freeze-drying to obtain a product with higher purity, improved relaxation rate and reduced renal toxicity.
本发明提供了一种钆特醇制备工艺,将钆特醇粗品加纯水溶解,使用数字超声仪进行间歇超声,超声操作的同时通入惰性气体,间歇期间缓慢滴加乙醇和/或异丙醇,停止超声后继续磁力搅拌1-2h,静置析晶,过滤并监测滤液电导率,最后通过冷冻干燥获得纯度较高弛豫率提高且肾毒性降低的产品。</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2022</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFAIKEotSCxKLMnMz1PITS3JyE9RyE9TSE9MyS9JLSnKz-FhYE1LzClO5YXS3AyKbq4hzh66qQX58anFBYnJqXmpJfHOfoaGJoYGphaW5o7GxKgBAGpnJX8</recordid><startdate>20220301</startdate><enddate>20220301</enddate><creator>WU ZUTI</creator><creator>ZHOU SHENGJUN</creator><creator>ZHU YIFAN</creator><creator>WANG YUXING</creator><creator>LU CUIJUN</creator><creator>WANG YINGHUI</creator><creator>FAN MINHUA</creator><creator>NIE LIANGDENG</creator><scope>EVB</scope></search><sort><creationdate>20220301</creationdate><title>Preparation method of gadotetrol</title><author>WU ZUTI ; ZHOU SHENGJUN ; ZHU YIFAN ; WANG YUXING ; LU CUIJUN ; WANG YINGHUI ; FAN MINHUA ; NIE LIANGDENG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN114105897A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2022</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>WU ZUTI</creatorcontrib><creatorcontrib>ZHOU SHENGJUN</creatorcontrib><creatorcontrib>ZHU YIFAN</creatorcontrib><creatorcontrib>WANG YUXING</creatorcontrib><creatorcontrib>LU CUIJUN</creatorcontrib><creatorcontrib>WANG YINGHUI</creatorcontrib><creatorcontrib>FAN MINHUA</creatorcontrib><creatorcontrib>NIE LIANGDENG</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WU ZUTI</au><au>ZHOU SHENGJUN</au><au>ZHU YIFAN</au><au>WANG YUXING</au><au>LU CUIJUN</au><au>WANG YINGHUI</au><au>FAN MINHUA</au><au>NIE LIANGDENG</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Preparation method of gadotetrol</title><date>2022-03-01</date><risdate>2022</risdate><abstract>The invention provides a gadotetrol preparation process, which comprises the following steps: adding pure water into a gadotetrol crude product for dissolving, performing intermittent ultrasonic treatment by using a digital ultrasonic instrument, introducing inert gas while performing ultrasonic operation, slowly dropwise adding ethanol and/or isopropanol during the intermittent period, stopping ultrasonic treatment, continuing magnetic stirring for 1-2 hours, standing for devitrification, filtering, and monitoring the conductivity of filtrate, thereby obtaining the gadotetrol. And finally, freeze-drying to obtain a product with higher purity, improved relaxation rate and reduced renal toxicity.
本发明提供了一种钆特醇制备工艺,将钆特醇粗品加纯水溶解,使用数字超声仪进行间歇超声,超声操作的同时通入惰性气体,间歇期间缓慢滴加乙醇和/或异丙醇,停止超声后继续磁力搅拌1-2h,静置析晶,过滤并监测滤液电导率,最后通过冷冻干燥获得纯度较高弛豫率提高且肾毒性降低的产品。</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Preparation method of gadotetrol |
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