Adding a certain compound to certain chemical reactions, such as: 175137-46-9, name is 5-Cyclopropyl-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 175137-46-9, category: pyrazoles-derivatives
To a solution of 2,4-difluoro-l -nitrobenzene (1.76 g, 11.1 mmol) and DIEA (1.93 ml, 11.1 mmol) in TEtaF (20 ml) was added dropwise a solution of 5-cyclopropyl-lH-pyrazol-3- amine (0.91 g, 7.39 mmol) in TEtaF (5 ml) at 25 C. After addition, the reaction mixture was stirred at 80 0C for 48 hours. The solvent was removed under reduced pressure and the resulted residue was purified by column chromatography (hexane : DCM : EtOAc = 2 : 1 : 1) to give the title compound as a yellow solid (0.62 g, 32%). NMR (400 MHz) 12.37 (s, IH), 9.83 (s, IH), 8.25 (m, IH), 7.98 (d, J= 11.2 Hz, IH), 6.75 (m, IH), 5.95 (s, IH), 1.90 (m, IH), 0.96 (m, 2H), 0.72 (m, 2H).
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Reference:
Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2006/87530; (2006); A1;,
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics