Brief introduction of 120014-07-5

120014-07-5, As the paragraph descriping shows that 120014-07-5 is playing an increasingly important role.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.120014-07-5,2-((1-Benzylpiperidin-4-yl)methylene)-5,6-dimethoxy-2,3-dihydro-1H-inden-1-one,as a common compound, the synthetic route is as follows.

To 200 mL of toluene were added 20 g of 1-benzyl-4-[(5,6-dimethoxy-1-indanon)-2-ylidene]methyl-piperidine and 2 g of 10% palladium-carbon. Hydrogenation was carried out with stirring for 5 hours at 0 to 1 C. and 0.8 to 1.0 MPa. HPLC Purity of the Reaction Solution: the desired compound/72.9%, the starting material/25.3%, the debenzylated product/1.8%.

120014-07-5, As the paragraph descriping shows that 120014-07-5 is playing an increasingly important role.

Reference£º
Patent; Eisai R&D Management Co., Ltd.; US2007/88055; (2007); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem