Novel technology of preparing thifluzamide from thiazole acid
The invention provides a novel technology of preparing thifluzamide from thiazole acid. The invention relates to a preparation method of a bactericide namely thifluzamide, and belongs to the technicalfield of chemistry. The invention discloses a one-step synthesis method of thifluzamide, and the syn...
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creator | WANG SHIYIN JIA FENGCONG WU XIAOXIA LIU-FU KANGHUA LIU SHIYONG PENG JUN |
description | The invention provides a novel technology of preparing thifluzamide from thiazole acid. The invention relates to a preparation method of a bactericide namely thifluzamide, and belongs to the technicalfield of chemistry. The invention discloses a one-step synthesis method of thifluzamide, and the synthesis method is simple and high efficient. According to the synthesis method, 2-methyl-4-trifluoromethyl-1,3-thiazole formic acid and 2,6-dibromo-trifluoromethoxyl aniline are taken as the primary raw materials, and the bactericide namely thifluzamide is synthesized in one step without any intermediate treatment in the presence of a catalyst. The novel technology has the advantages that the step is simple, there are few post treatment steps, and the reaction period is shortened.
种由噻唑酸制备噻呋酰胺的新型工艺。本发明涉及种杀菌剂噻呋酰胺的制备方法,属于化学技术领域。本发明公开了种简单高效步法制备噻呋酰胺的合成方法。以2-甲基-4-三氟甲基-1,3-噻唑甲酸、2,6-二溴-4-三氟甲氧基苯胺为起始原料,在催化剂存在的条件下,中间不处理步法合成杀菌剂噻呋酰胺。其优点是:步骤简单,反应后处理程序比较少,缩短了反应周期。 |
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种由噻唑酸制备噻呋酰胺的新型工艺。本发明涉及种杀菌剂噻呋酰胺的制备方法,属于化学技术领域。本发明公开了种简单高效步法制备噻呋酰胺的合成方法。以2-甲基-4-三氟甲基-1,3-噻唑甲酸、2,6-二溴-4-三氟甲氧基苯胺为起始原料,在催化剂存在的条件下,中间不处理步法合成杀菌剂噻呋酰胺。其优点是:步骤简单,反应后处理程序比较少,缩短了反应周期。</description><language>chi ; eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2018</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=20180522&DB=EPODOC&CC=CN&NR=108059625A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20180522&DB=EPODOC&CC=CN&NR=108059625A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>WANG SHIYIN</creatorcontrib><creatorcontrib>JIA FENGCONG</creatorcontrib><creatorcontrib>WU XIAOXIA</creatorcontrib><creatorcontrib>LIU-FU KANGHUA</creatorcontrib><creatorcontrib>LIU SHIYONG</creatorcontrib><creatorcontrib>PENG JUN</creatorcontrib><title>Novel technology of preparing thifluzamide from thiazole acid</title><description>The invention provides a novel technology of preparing thifluzamide from thiazole acid. The invention relates to a preparation method of a bactericide namely thifluzamide, and belongs to the technicalfield of chemistry. The invention discloses a one-step synthesis method of thifluzamide, and the synthesis method is simple and high efficient. According to the synthesis method, 2-methyl-4-trifluoromethyl-1,3-thiazole formic acid and 2,6-dibromo-trifluoromethoxyl aniline are taken as the primary raw materials, and the bactericide namely thifluzamide is synthesized in one step without any intermediate treatment in the presence of a catalyst. The novel technology has the advantages that the step is simple, there are few post treatment steps, and the reaction period is shortened.
种由噻唑酸制备噻呋酰胺的新型工艺。本发明涉及种杀菌剂噻呋酰胺的制备方法,属于化学技术领域。本发明公开了种简单高效步法制备噻呋酰胺的合成方法。以2-甲基-4-三氟甲基-1,3-噻唑甲酸、2,6-二溴-4-三氟甲氧基苯胺为起始原料,在催化剂存在的条件下,中间不处理步法合成杀菌剂噻呋酰胺。其优点是:步骤简单,反应后处理程序比较少,缩短了反应周期。</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2018</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLD1yy9LzVEoSU3OyMvPyU-vVMhPUygoSi1ILMrMS1coychMyymtSszNTElVSCvKzwWJJFbl56QqJCZnpvAwsKYl5hSn8kJpbgZFN9cQZw_d1IL8-NTigsTk1LzUknhnP0MDCwNTSzMjU0djYtQAAFGcMJQ</recordid><startdate>20180522</startdate><enddate>20180522</enddate><creator>WANG SHIYIN</creator><creator>JIA FENGCONG</creator><creator>WU XIAOXIA</creator><creator>LIU-FU KANGHUA</creator><creator>LIU SHIYONG</creator><creator>PENG JUN</creator><scope>EVB</scope></search><sort><creationdate>20180522</creationdate><title>Novel technology of preparing thifluzamide from thiazole acid</title><author>WANG SHIYIN ; JIA FENGCONG ; WU XIAOXIA ; LIU-FU KANGHUA ; LIU SHIYONG ; PENG JUN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN108059625A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2018</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>WANG SHIYIN</creatorcontrib><creatorcontrib>JIA FENGCONG</creatorcontrib><creatorcontrib>WU XIAOXIA</creatorcontrib><creatorcontrib>LIU-FU KANGHUA</creatorcontrib><creatorcontrib>LIU SHIYONG</creatorcontrib><creatorcontrib>PENG JUN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WANG SHIYIN</au><au>JIA FENGCONG</au><au>WU XIAOXIA</au><au>LIU-FU KANGHUA</au><au>LIU SHIYONG</au><au>PENG JUN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Novel technology of preparing thifluzamide from thiazole acid</title><date>2018-05-22</date><risdate>2018</risdate><abstract>The invention provides a novel technology of preparing thifluzamide from thiazole acid. The invention relates to a preparation method of a bactericide namely thifluzamide, and belongs to the technicalfield of chemistry. The invention discloses a one-step synthesis method of thifluzamide, and the synthesis method is simple and high efficient. According to the synthesis method, 2-methyl-4-trifluoromethyl-1,3-thiazole formic acid and 2,6-dibromo-trifluoromethoxyl aniline are taken as the primary raw materials, and the bactericide namely thifluzamide is synthesized in one step without any intermediate treatment in the presence of a catalyst. The novel technology has the advantages that the step is simple, there are few post treatment steps, and the reaction period is shortened.
种由噻唑酸制备噻呋酰胺的新型工艺。本发明涉及种杀菌剂噻呋酰胺的制备方法,属于化学技术领域。本发明公开了种简单高效步法制备噻呋酰胺的合成方法。以2-甲基-4-三氟甲基-1,3-噻唑甲酸、2,6-二溴-4-三氟甲氧基苯胺为起始原料,在催化剂存在的条件下,中间不处理步法合成杀菌剂噻呋酰胺。其优点是:步骤简单,反应后处理程序比较少,缩短了反应周期。</abstract><oa>free_for_read</oa></addata></record> |
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title | Novel technology of preparing thifluzamide from thiazole acid |
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