Some scientific research about 2-Aminopyrimidin-4(1H)-one

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,108-53-2, its application will become more common.

Adding a certain compound to certain chemical reactions, such as: 108-53-2, 2-Aminopyrimidin-4(1H)-one, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 108-53-2, blongs to pyrimidines compound. Recommanded Product: 2-Aminopyrimidin-4(1H)-one

The synthetic route of this comparative example is as follows:Isocytosine (4g) and phosphorus oxybromide (10g) were mixed well at room temperature,The reaction was stirred at 80 C for 2 hours,Then slowly warmed to 135 ,The reaction was held at 135 C until the reaction was complete.The reaction was cooled to 0 C and the pH was adjusted to 12 and 1 g of product was filtered off (16% yield).Elemental analysis showed that the yellow solid could be identified as 2-amino-4-bromopyrimidine. c

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,108-53-2, its application will become more common.

Reference:
Patent; Shanghai Zaiqi Biological Co., Ltd.; Wang Zhiguo; Song Yanhong; Ma Xiujuan; Tian Beibei; Li Shijiang; Li Chao; Li Qiang; Li Tao; (5 pag.)CN106632077; (2017); A;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia