{"id":3556,"date":"2021-04-21T09:28:54","date_gmt":"2021-04-21T01:28:54","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=3556"},"modified":"2021-04-21T09:28:54","modified_gmt":"2021-04-21T01:28:54","slug":"analyzing-the-synthesis-route-of-3-iodo-14-dimethyl-1h-pyrazole","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=3556","title":{"rendered":"Analyzing the synthesis route of 3-Iodo-1,4-dimethyl-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. 1395443-04-5, name is 3-Iodo-1,4-dimethyl-1H-pyrazole, A new synthetic method of this compound is introduced below., <a href=\"https:\/\/www.ambeed.com\/products\/1395443-04-5.html\">name: 3-Iodo-1,4-dimethyl-1H-pyrazole<\/a><\/p>\n<p>A mixture of 3-iodo- 1 ,4-dimethyl- pyrazole (5 g, 22.52 mmol), tert-butyl carbamate (3.43 g, 29.28 mmol), Cul (2.14 g, 11.26 rnmol), K2CO3 (6.22 g, 45.04 mmol) and (lS,2S)-Nl,N2-dimemylcyclohexane-L2-diamine (1.6 g, 11.26 mmol) in 1,4- dioxane (60 mL) was degassed and purged with N2 for 3 times, and then the mixture solution was stirred at 1 10 C for 12 h under N2. To the reaction solution was added water (80 mL), extracted with EtO Ac (30 mL x 3), organic layers were combined, washed with brine (30 mL), dried over Na2SO.i, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (PE: EtOAc = 5: 1 to 3: 1) to give tert-butyl N-(1,4-dimethylpyrazol-3-yl)carbamate as a light brown solid. lH NMR (400 MHz, ( DC -.): delta ppm 7,06 (s, 1 H), 6.44 (br, s,, 1 H), 3.71 &#8211; 3.81 (m, 3 H), 1.98 (s, 3 H), 1.48 (s, 9 H).<\/p>\n<p>The synthetic route of 1395443-04-5 has been constantly updated, and we look forward to future research findings.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The synthetic route of 1395443-04-5 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":[548,131],"tags":[127],"class_list":["post-3556","post","type-post","status-publish","format-standard","hentry","category-1395443-04-5","category-pyrazoles-derivatives","tag-m-w200-300"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Analyzing the synthesis route of 3-Iodo-1,4-dimethyl-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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