Discovery of 274-82-8

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route [1,2,4]Triazolo[4,3-a]pyrazine, its application will become more common.

Synthetic Route of 274-82-8,Some common heterocyclic compound, 274-82-8, name is [1,2,4]Triazolo[4,3-a]pyrazine, molecular formula is C5H4N4, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To a solution of [l ,2,4]triazolo[4,3-a]pyrazine (1.50 g) in MeOH ( 150 mL) was added Pt02 ( 1.10 g) and 10% Pd/C (0.46 g) at rt. The suspension was stirred under H2 at room temperature for 16 h and filtered. The filtrate was concentrated in vacuo andthe residue was chromatographed with a silica gel column to give the title compound (0.18 g, 1 1.54 %). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 125.1 (M+l ).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route [1,2,4]Triazolo[4,3-a]pyrazine, its application will become more common.

Reference:
Patent; SUNSHINE LAKE PHARMA CO., LTD.; ZHANG, Jiancun; ZHANG, Yingjun; ZHANG, Weihong; LIU, Bing; ZHANG, Jiquan; LIU, Jinlei; ZHANG, Lu; WO2013/71697; (2013); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

The important role of 274-82-8

The synthetic route of 274-82-8 has been constantly updated, and we look forward to future research findings.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 274-82-8, name is [1,2,4]Triazolo[4,3-a]pyrazine belongs to Pyrazines compound, it is a common compound, a new synthetic route is introduced below. Product Details of 274-82-8

To a solution of [1,2,4]triazolo[4,3-a]pyrazine (1.50 g) in MeOH (150 mL) was added PtO2 (1.10 g) and 10% Pd/C (0.46 g) at rt. The suspension was stirred under H2 at room temperature for 16 h and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column to give the title compound (0.18 g, 11.54%). The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 125.1 (M+1).

The synthetic route of 274-82-8 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; SUNSHINE LAKE PHARMA CO., LTD.; Zhang, Jiancun; Zhang, Yingjun; Zhang, Weihong; Liu, Bing; Zhang, Jiquan; Liu, Jinlei; Zhang, Lu; US2014/228361; (2014); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem