Preparation method of dinaverine hydrochloride
The invention relates to a preparation method of dinaverine hydrochloride, the methdo comprises the following steps: using 2, 2-diphenyl-2-glycolic acid as a raw material, adding reagents such as thionyl chloride and the like, reacting carboxyl in 2, 2-diphenyl-2-glycolic acid molecules to form acyl...
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creator | ZHANG YUNXIAN GUO CHUANZHEN NING SHUQUN KONG MEI LIU QUANCAI KONG QINGWEN FANG MINGFENG |
description | The invention relates to a preparation method of dinaverine hydrochloride, the methdo comprises the following steps: using 2, 2-diphenyl-2-glycolic acid as a raw material, adding reagents such as thionyl chloride and the like, reacting carboxyl in 2, 2-diphenyl-2-glycolic acid molecules to form acyl chloride and reacting benzyl alcohol to form benzyl chloride in one step; adding dimethylaminoethanol under certain conditions, reacting with acyl chloride to obtain ester, adding 2-ethyl butanol, controlling reaction conditions, and reacting with benzyl chloride to obtain denaverine hydrochloride; the reaction route solves the problems that the esterification solid-liquid reaction speed is low and high-temperature reaction is needed, the reaction condition is mild, the speed is high, and the yield is high.
本发明涉及一种盐酸地那维林的制备方法,该方法使用2,2-二苯基-2-羟基乙酸为原料,加入氯化亚砜等试剂,一步将2,2-二苯基-2-羟基乙酸分子中的羧基反应成酰氯,苄醇反应成苄氯;然后在一定的条件下,加入二甲氨基乙醇,与酰氯反应得到酯,然后加入2-乙基丁醇,控制反应条件,与苄氯反应得到盐酸地那维林;该反应路线解决了成酯固液反应速度慢且需要高温反应的问题,反应条件温和,且速度快,收率高。 |
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本发明涉及一种盐酸地那维林的制备方法,该方法使用2,2-二苯基-2-羟基乙酸为原料,加入氯化亚砜等试剂,一步将2,2-二苯基-2-羟基乙酸分子中的羧基反应成酰氯,苄醇反应成苄氯;然后在一定的条件下,加入二甲氨基乙醇,与酰氯反应得到酯,然后加入2-乙基丁醇,控制反应条件,与苄氯反应得到盐酸地那维林;该反应路线解决了成酯固液反应速度慢且需要高温反应的问题,反应条件温和,且速度快,收率高。</description><language>chi ; eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; 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=20220128&DB=EPODOC&CC=CN&NR=113979873A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20220128&DB=EPODOC&CC=CN&NR=113979873A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>ZHANG YUNXIAN</creatorcontrib><creatorcontrib>GUO CHUANZHEN</creatorcontrib><creatorcontrib>NING SHUQUN</creatorcontrib><creatorcontrib>KONG MEI</creatorcontrib><creatorcontrib>LIU QUANCAI</creatorcontrib><creatorcontrib>KONG QINGWEN</creatorcontrib><creatorcontrib>FANG MINGFENG</creatorcontrib><title>Preparation method of dinaverine hydrochloride</title><description>The invention relates to a preparation method of dinaverine hydrochloride, the methdo comprises the following steps: using 2, 2-diphenyl-2-glycolic acid as a raw material, adding reagents such as thionyl chloride and the like, reacting carboxyl in 2, 2-diphenyl-2-glycolic acid molecules to form acyl chloride and reacting benzyl alcohol to form benzyl chloride in one step; adding dimethylaminoethanol under certain conditions, reacting with acyl chloride to obtain ester, adding 2-ethyl butanol, controlling reaction conditions, and reacting with benzyl chloride to obtain denaverine hydrochloride; the reaction route solves the problems that the esterification solid-liquid reaction speed is low and high-temperature reaction is needed, the reaction condition is mild, the speed is high, and the yield is high.
本发明涉及一种盐酸地那维林的制备方法,该方法使用2,2-二苯基-2-羟基乙酸为原料,加入氯化亚砜等试剂,一步将2,2-二苯基-2-羟基乙酸分子中的羧基反应成酰氯,苄醇反应成苄氯;然后在一定的条件下,加入二甲氨基乙醇,与酰氯反应得到酯,然后加入2-乙基丁醇,控制反应条件,与苄氯反应得到盐酸地那维林;该反应路线解决了成酯固液反应速度慢且需要高温反应的问题,反应条件温和,且速度快,收率高。</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2022</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNALKEotSCxKLMnMz1PITS3JyE9RyE9TSMnMSyxLLcrMS1XIqEwpyk_OyMkvykxJ5WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8c5-hobGluaWFubGjsbEqAEAMDArJQ</recordid><startdate>20220128</startdate><enddate>20220128</enddate><creator>ZHANG YUNXIAN</creator><creator>GUO CHUANZHEN</creator><creator>NING SHUQUN</creator><creator>KONG MEI</creator><creator>LIU QUANCAI</creator><creator>KONG QINGWEN</creator><creator>FANG MINGFENG</creator><scope>EVB</scope></search><sort><creationdate>20220128</creationdate><title>Preparation method of dinaverine hydrochloride</title><author>ZHANG YUNXIAN ; GUO CHUANZHEN ; NING SHUQUN ; KONG MEI ; LIU QUANCAI ; KONG QINGWEN ; FANG MINGFENG</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN113979873A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2022</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>ZHANG YUNXIAN</creatorcontrib><creatorcontrib>GUO CHUANZHEN</creatorcontrib><creatorcontrib>NING SHUQUN</creatorcontrib><creatorcontrib>KONG MEI</creatorcontrib><creatorcontrib>LIU QUANCAI</creatorcontrib><creatorcontrib>KONG QINGWEN</creatorcontrib><creatorcontrib>FANG MINGFENG</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>ZHANG YUNXIAN</au><au>GUO CHUANZHEN</au><au>NING SHUQUN</au><au>KONG MEI</au><au>LIU QUANCAI</au><au>KONG QINGWEN</au><au>FANG MINGFENG</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Preparation method of dinaverine hydrochloride</title><date>2022-01-28</date><risdate>2022</risdate><abstract>The invention relates to a preparation method of dinaverine hydrochloride, the methdo comprises the following steps: using 2, 2-diphenyl-2-glycolic acid as a raw material, adding reagents such as thionyl chloride and the like, reacting carboxyl in 2, 2-diphenyl-2-glycolic acid molecules to form acyl chloride and reacting benzyl alcohol to form benzyl chloride in one step; adding dimethylaminoethanol under certain conditions, reacting with acyl chloride to obtain ester, adding 2-ethyl butanol, controlling reaction conditions, and reacting with benzyl chloride to obtain denaverine hydrochloride; the reaction route solves the problems that the esterification solid-liquid reaction speed is low and high-temperature reaction is needed, the reaction condition is mild, the speed is high, and the yield is high.
本发明涉及一种盐酸地那维林的制备方法,该方法使用2,2-二苯基-2-羟基乙酸为原料,加入氯化亚砜等试剂,一步将2,2-二苯基-2-羟基乙酸分子中的羧基反应成酰氯,苄醇反应成苄氯;然后在一定的条件下,加入二甲氨基乙醇,与酰氯反应得到酯,然后加入2-乙基丁醇,控制反应条件,与苄氯反应得到盐酸地那维林;该反应路线解决了成酯固液反应速度慢且需要高温反应的问题,反应条件温和,且速度快,收率高。</abstract><oa>free_for_read</oa></addata></record> |
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title | Preparation method of dinaverine hydrochloride |
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