1450-93-7, Adding some certain compound to certain chemical reactions, such as: 1450-93-7, name is 1H-imidazol-2-amine sulfate(2:1), 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 1450-93-7.
2-Aminoimidazole sulfate (1.53 g) is dissolved in 0.97 mL of concentrated HCI, 1 mL of water, and 3 mL of acetic acid. The resulting solution is cooled to 0 oC. A solution 799 mg of NaN02 in 2 mL of water is added dropwise, and the internal temperature is maintained below 5C. The resulting yellow-brown solution is stirred for 30 minutes at 0 o20 C. In a separate flask equipped with a mechanical stirrer a mixture of 1.65 g of 1, 4-diallyl-l, 2,3, 4- tetrahydroquinoxaline, 1.9 g of sodium acetate and 10 mL of acetic acid is cooled to 0 C. The diazonium solution is added slowly to this slurry while stirring. After the addition is complete, the resulting red suspension is stirred for 1 hour at 0 oC. The dark reaction mixture is poured into a beaker containing 10 g of ice. Aqueous NaOH (20%) is added to the suspension slowly until pH 6.5 is reached. The mixture is filtered and the dark solid is dried. (E)-6-((lH-imidazol- 2-yl)diazenyl)-l,4-diallyl-l,2,3,4-tetrahydroquinoxaline (2.3g) is used in the next step without further purification.
Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 1450-93-7.
Reference:
Patent; NOXELL CORPORATION; MURPHY, Bryan Patrick; ZHANG, Guiru; ZHAO, Jielu; (106 pag.)WO2018/53034; (2018); A1;,
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem