The origin of a common compound about 4-Bromo-3,5-dimethylpyrazole

The synthetic route of 3398-16-1 has been constantly updated, and we look forward to future research findings.

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. 3398-16-1, name is 4-Bromo-3,5-dimethylpyrazole, A new synthetic method of this compound is introduced below., Quality Control of 4-Bromo-3,5-dimethylpyrazole

A mixture of tert-butyl 3-(cyanomethyl)-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]azetidine-1-carboxylate (381 mg, 0.981 mmol, from Example 1, step 2), 4-bromo-3,5-dimethyl-1H-pyrazole (206 mg, 1.18 mmol), tetrakis(triphenylphosphine)palladium(0) (110 mg, 0.098 mmol) and sodium carbonate (310 mg, 2.9 mmol) in 1,4-dioxane (10 mL) and water (5 mL) was purged with N2 and stirred at 110° C. for 2 h. The reaction mixture was filtered, diluted with EtOAc, then washed with water. The organic layer was concentrated and purified on silica gel (eluting with 0-100percent EtOAc/hexanes followed by 0-10percent MeOH/ dichloromethane) to give tert-butyl 3-(cyanomethyl)-3-(3?,5?-dimethyl-1H,1?H-4,4?-bipyrazol-1-yl)azetidine-1-carboxylate (90 mg, 26percent). LCMS calculated for C18H25N6O2 (M+H)+: m/z=357.2. Found: 357.2.

The synthetic route of 3398-16-1 has been constantly updated, and we look forward to future research findings.