Category: 19733-56-3

Electric Literature of 19733-56-3, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 19733-56-3, Name is 4-(Piperidin-3-yl)aniline, molecular formula is C11H16N2. In a Patent，once mentioned of 19733-56-3

The invention belongs to the field of drug synthesis, relates to a kind of ACDS nepal pulls the handkerchief cloth intermediate 4 – (piperidin – 3 – yl) aniline of the preparation method. This method uses the halogenated 1 – benzyl – 3 – (4 – nitrophenyl) pyridine as starting material, in the presence of Pd/C can be prepared by catalytic hydrogenation of 4 – (piperidin – 3 – yl) aniline, the method has low cost, high yield, can effectively avoid the N – (4 – (pyridine – 3 – yl) phenyl) hydroxylamine impurities, easy operation, safety and environmental protection, and is suitable for large-scale production, in order to further process for preparing high-purity nepal pulls the handkerchief cloth provide technical support. (by machine translation)

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Electric Literature of 19733-56-3, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 19733-56-3, in my other articles.

Reference：
Piperidine – Wikipedia,
Piperidine | C5H10509N – PubChem

Electric Literature of 19733-56-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.19733-56-3, Name is 4-(Piperidin-3-yl)aniline, molecular formula is C11H16N2. In a Patent，once mentioned of 19733-56-3

The present invention relates to novel procedures and novel intermediates useful in the synthesis of Niraparib or any salt thereof.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 19733-56-3 is helpful to your research. Electric Literature of 19733-56-3

Reference：
Piperidine – Wikipedia,
Piperidine | C5H10504N – PubChem

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 19733-56-3, name is 4-(Piperidin-3-yl)aniline, introducing its new discovery. SDS of cas: 19733-56-3

The invention discloses a compound 2 – [4 – ((3S) – 3 – piperidinyl) phenyl] – 2H – indazole – 7 – carboxamide preparation method, through the 4 – nitro phenylpyridyl with reaction produced animal pen halogenphenmethyl season ammonium salt, by sodium borohydride reduction of the pyridine quaternary ammonium salt, in the palladium reagent obtained under the action of the 3 – (4 – aminophenyl) piperidine, in the chiral reagent obtained under the action of the (S)- 3 – (4 – halophenyl) piperidine, with 3 – formyl – 2 – nitro-benzoic acid methyl ester condensation and in sodium azide formed under the action of powder medicine, after preparing the amine Niraparib (molecular entity is: 2 – [4 – ((3S) – 3 – piperidinyl) phenyl] – 2H – indazole – 7 – carboxamide). (by machine translation)

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 19733-56-3 is helpful to your research. category: piperidines

Reference：
Piperidine – Wikipedia,
Piperidine | C5H10507N – PubChem

Related Products of 19733-56-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.19733-56-3, Name is 4-(Piperidin-3-yl)aniline, molecular formula is C11H16N2. In a Patent，once mentioned of 19733-56-3

The invention discloses a compound 2 – [4 – ((3S) – 3 – piperidinyl) phenyl] – 2H – indazole – 7 – carboxamide preparation method, benzyl protection of trifluoromethanesulfonic anhydride – piperidone in under the action of the generated 3 – trifluoromethanesulfonic anhydride of the piperidone, with the Suzuki reaction to the nitrobenzene boric acid occurred after the coupling of the product obtained, and then under the action of the palladium reagent to obtain 3 – (4 – aminophenyl) piperidine, with chiral resolving agent made of (S)- 3 – (4 – halophenyl) piperidine, with 3 – formyl – 2 – nitro-benzoic acid methyl ester condensation and in sodium azide formed under the action of powder medicine, after preparing the amine Niraparib (molecular entity is: 2 – [4 – ((3S) – 3 – piperidinyl) phenyl] – 2H – indazole – 7 – carboxamide). (by machine translation)

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 19733-56-3

Reference：
Piperidine – Wikipedia,
Piperidine | C5H10508N – PubChem

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.19733-56-3,4-(Piperidin-3-yl)aniline,as a common compound, the synthetic route is as follows.

To a mixture of 4-(piperidin-3-yl) aniline (Compound 16) (0.5 g) in acetone (5 mL), succinic acid (0.36 g) was charged at reflux temperature. The reaction mass was stirred at reflux temperature for 30 minute. The reaction mass was cooled to 20-25C and stirred further for 3 h. The solid obtained was filtered, washed with acetone (3 mL) and dried under vacuum at 50-55C to afford the titled compound (Yield: 0.63 g; HPLC Purity: >95.0% ).

19733-56-3, As the paragraph descriping shows that 19733-56-3 is playing an increasingly important role.

Reference£º
Patent; TEVA PHARMACEUTICALS USA, INC.; TEVA PHARMACEUTICALS INTERNATIIONAL GMBH; LUTHRA, Parven, Kumar; VASOYA, Sanjay, Lakhabhai; PATIL, Bhatu, Tumba; TANEJA, Amit, Kumar; SRIVASTAV, Naveen, Chandra; SINGH, Rinku; (63 pag.)WO2019/36441; (2019); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem