Extended knowledge of 2-(1-Benzylpiperidin-4-yl)-2-propanol

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Electric Literature of 299428-04-9, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 299428-04-9, in my other articles.

Electric Literature of 299428-04-9, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 299428-04-9, Name is 2-(1-Benzylpiperidin-4-yl)-2-propanol, molecular formula is C15H23NO. In a Patent,once mentioned of 299428-04-9

The present invention is directed to certain compounds useful as phosphodiesterase 10 (PDE10) inhibitors that have the formula where R1, R2, R3, R4, X, Y and Z are as defined herein, pharmaceutical compositions containing such compounds and processes for preparing such compounds. The invention is also directed to methods of treating diseases mediated by PDE10, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Electric Literature of 299428-04-9, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 299428-04-9, in my other articles.

Reference:
Piperidine – Wikipedia,
Piperidine | C5H18944N – PubChem

 

Some tips on 299428-04-9

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With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.299428-04-9,2-(1-Benzylpiperidin-4-yl)-2-propanol,as a common compound, the synthetic route is as follows.

The benzyl protecting group was removed with palladium, 10 wt. % on activated carbon and placing the reaction vessel under hydrogen (g) overnight. Upon completion, the reaction mixture was filtered through Celite. The filtrate was concentrated to produce 2-(piperidin-4-yl)propan-2-ol., 299428-04-9

As the paragraph descriping shows that 299428-04-9 is playing an increasingly important role.

Reference£º
Patent; Hu, Essa; Kunz, Roxanne; Nixey, Tom; Hitchcock, Stephen; US2009/62291; (2009); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem