{"id":1589,"date":"2021-01-28T04:44:53","date_gmt":"2021-01-27T20:44:53","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=1589"},"modified":"2021-01-28T04:44:53","modified_gmt":"2021-01-27T20:44:53","slug":"the-important-role-of-578008-32-9","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=1589","title":{"rendered":"The important role of 578008-32-9"},"content":{"rendered":"<p>Adding a certain compound to certain chemical reactions, such as: 578008-32-9, name is tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound  578008-32-9, <a href=\"https:\/\/www.ambeed.com\/products\/578008-32-9.html\">Application In Synthesis of  tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate<\/a><\/p>\n<p>To a 20 mL vial was added tert-butyl (1R,3s,55)-3-((7-chloro-1,6-naphthyridin-5- yl)amino)-8-azabicyclo[3.2.ljoctane-8-carboxylate (474.6 mg, 1.22 mmol), tert-butyl 3-amino-S -methyl- 1H-pyrazole- 1 -carboxylate (289 mg, 1.46 mmol), chloro [2- (dicyclohexylphosphino)-3 ,6-dimethoxy-2?-4?-6?-tri- (58 mg, 0.073 mmol), and cesium carbonate (517 mg, 1.59 mmol). The vial was sealed with a rubber septum and the atmosphere was flushed with nitrogen. Dioxane (6.10 mL) was then added via syringe, and the septum was quickly replaced with a white cap. The reaction mixture was heatedto 110 C and stirred for 26 h and cooled to RT. The suspension was diluted with water and brine and extracted with EtOAc (4 x 20 mL). The combined organic fractions were dried over sodium sulfate, filtered, and concentrated to afford a brown foamy solid which was used directly in the next step. (m\/z): [M+Hj calcd for C29H39N704 550.31, found550.8.<\/p>\n<p>In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate, other downstream synthetic routes, hurry up and to see.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate, other downstream synthetic routes, hurry up and to see.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[330,131],"tags":[126],"class_list":["post-1589","post","type-post","status-publish","format-standard","hentry","category-578008-32-9","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>The important role of 578008-32-9<\/title>\n<meta name=\"description\" content=\"Adding a certain compound to certain chemical reactions, such as: 578008-32-9, name is tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. 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Here is a downstream synthesis route of the compound 578008-32-9, Application In Synthesis of tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.pyrazoles-derivatives.com\/?p=1589","og_locale":"en_US","og_type":"article","og_title":"The important role of 578008-32-9","og_description":"Adding a certain compound to certain chemical reactions, such as: 578008-32-9, name is tert-Butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. 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