Brief introduction of 2-Amino-1-(piperidin-1-yl)ethanone hydrochloride

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Reference of 5437-48-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.5437-48-9, Name is 2-Amino-1-(piperidin-1-yl)ethanone hydrochloride, molecular formula is C7H15ClN2O. In a Article，once mentioned of 5437-48-9

A general and practical synthetic protocol for the direct transformation of unreactive C(sp3)-H bonds to C(sp3)-CN bonds has been developed. The homolytic cleavage of the C-H bond is initiated by photo-excited benzophenone, and the resulting carbon radical subsequently reacts with tosyl cyanide to afford the corresponding nitrile in a highly efficient manner. The present methodology is widely applicable to various starting materials including ethers, alcohols, amine derivatives, alkanes, and alkylbenzenes. This newly developed C-H cyanation protocol provides a powerful tool for selective one-carbon elongation for the construction of architecturally complex molecules. Georg Thieme Verlag Stuttgart – New York.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H10862N – PubChem