With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.2166-31-6,6-Phenylpyridazin-3(2H)-one,as a common compound, the synthetic route is as follows.
135 ml (135 mmole) of a solution of phenylmagnesium bromide (IM) in THF was added to a hot suspension of 6-phenylpyridazinone compound 7.8g (45 mmole) in dry toluene (50 ml). The mixture was refluxed for 8h, left overnight at ambient temperature, then decomposed with a saturated solution of ammonium chloride. The organic layer was separated, and the aqueous
2166-31-6, As the paragraph descriping shows that 2166-31-6 is playing an increasingly important role.
Reference£º
Patent; NORTHWESTERN UNIVERSITY; WO2007/127474; (2007); A2;,
Pyridazine – Wikipedia
Pyridazine | C4H4N2 – PubChem