{"id":5187,"date":"2021-07-06T04:06:03","date_gmt":"2021-07-05T20:06:03","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=5187"},"modified":"2021-07-06T04:06:03","modified_gmt":"2021-07-05T20:06:03","slug":"some-tips-on-121507-34-4","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=5187","title":{"rendered":"Some tips on 121507-34-4"},"content":{"rendered":"<p>Adding a certain compound to certain chemical reactions, such as: 121507-34-4, name is 5-Isopropoxy-1H-pyrazol-3-amine, 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  121507-34-4, <a href=\"https:\/\/www.ambeed.com\/products\/121507-34-4.html\">Safety of 5-Isopropoxy-1H-pyrazol-3-amine<\/a><\/p>\n<p>Method 2; 2,5-Dichloro-N-(5-isopropoxy-lH-pyrazol-3-yl)pyrimidin-4-amine; A solution of 2,4,5-trichloropyrimidine (533 mg, 2.93 mmol), 5-isopropoxy-lH- pyrazol-3 -amine (413 mg, 2.93 mmol) and triethylamine (0.49 ml) in TetaF (5 ml) was stirred at room temperature for 10 hours. Solvent was removed and EtOAc was added. The solution was washed with water and dried over anhydrous sodium sulfate and was concentrated to give title compound as a white solid (582 mg, 69%). LC-MS, 246 (M-42); 1H nuMR (CDCl3) delta 8.19 (s, IH), 7.80 (s, IH)5 5.79 (s, IH), 4.65 (m, IH), 1.30 (d, 6H).<\/p>\n<p>If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.<\/p>\n<p>Reference:<br \/><a href=\"http:\/\/v3.espacenet.com\/textdoc?DB=EPODOC&#038;IDX=WO2007049041&#038;F=0\">Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2007\/49041; (2007); A1;<\/a>,<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/p>\n","protected":false},"excerpt":{"rendered":"<p>If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[346,131],"tags":[126],"class_list":["post-5187","post","type-post","status-publish","format-standard","hentry","category-121507-34-4","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>Some tips on<\/title>\n<meta name=\"description\" content=\"Adding a certain compound to certain chemical reactions, such as: 121507-34-4, name is 5-Isopropoxy-1H-pyrazol-3-amine, 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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