{"id":3359,"date":"2021-04-13T00:00:00","date_gmt":"2021-04-12T16:00:00","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=3359"},"modified":"2021-04-13T00:00:00","modified_gmt":"2021-04-12T16:00:00","slug":"application-of-5-chloro-3-trifluoromethyl-1h-pyrazole","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=3359","title":{"rendered":"Application of 5-Chloro-3-(trifluoromethyl)-1H-pyrazole"},"content":{"rendered":"<p>Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 131797-35-8, name is 5-Chloro-3-(trifluoromethyl)-1H-pyrazole, A new synthetic method of this compound is introduced below., <a href=\"https:\/\/www.ambeed.com\/products\/131797-35-8.html\">Product Details of 131797-35-8<\/a><\/p>\n<p>To a mixture of 7-(chloromethyl)-3-propanoyl-2-(trifluoromethyl)-5H-[l,3]thiazolo[3,2- a]pyrimidin-5-one (15 mg, 0.05mmol) in acetonitrile (3 mL, 57.1mmol) was added potassium carbonate (13 mg, 0.09 mmol) and 5-chloro-3-(trifluoromethyl)-lH-pyrazole (10 mg, 0.06 mmol). The resulting mixture was stirred for 2 h at 80 C. After filtration and concentration, the residue was purified by chromatography with ethyl acetate\/petroleum ether (1\/3) to afford 7-[[5-chloro-3-(trifluoromethyl)-lH- pyrazol-l-yl]methyl]-3-propanoyl-2-(trifluoromethyl)-5H-[l,3]thiazolo[3,2-a]pyrimidin-5-one (4.5 mg, 21%) as a light brown solid. LCMS (ESI): M+H+ = 459.0; lU NMR (400 MHz, CDC13) delta 6.60 (s, 1H), 5.83 (s, 1H), 5.31 (s, 2H), 2.97-2.83 (m, 2H), 1.29-1.25 (m, 3H).<\/p>\n<p>The synthetic route of 131797-35-8 has been constantly updated, and we look forward to future research findings.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The synthetic route of 131797-35-8 has been constantly updated, and we look forward to future research findings.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[220,131],"tags":[126],"class_list":["post-3359","post","type-post","status-publish","format-standard","hentry","category-131797-35-8","category-pyrazoles-derivatives","tag-m-w100-200"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Application of 5-Chloro-3-(trifluoromethyl)-1H-pyrazole<\/title>\n<meta name=\"description\" content=\"Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. 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