Properties and Exciting Facts About Methyl 1-benzyl-3-oxopiperidine-4-carboxylate

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 175406-94-7

Synthetic Route of 175406-94-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.175406-94-7, Name is Methyl 1-benzyl-3-oxopiperidine-4-carboxylate, molecular formula is C14H17NO3. In a Article,once mentioned of 175406-94-7

Ring transformation of 2-cyanoimido-3-methyl-1,3-oxazolidine (10) yielded 5-amino-3-[N-(2-hydroxyethyl)-N-methyl] amino-1H-1,2,4-triazole (6) that was ring closed with different beta-keto esters to 2-[N-(2-hydroxyethyl)-N-methyl]amino-1,2,4-triazolo[1,5-a]pyrimidinones (4). Cyclisation of derivatives 4 led to imidazo[2?,1?:3,4][1,2,4]triazolo[1,5-a]pyrimidines (2) and imidazo[1?,2?:2,3][1,2,4]triazolo[1,5-a]pyrimidines (3) representing 10 novel ring systems, Besides spectroscopical evidence of structure of derivatives 2 and 3 X-ray diffraction analysis of derivative 2b was also performed.

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 175406-94-7

Reference:
Piperidine – Wikipedia,
Piperidine | C5H20451N – PubChem