Extended knowledge of Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 62208-68-8, Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione.

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 62208-68-8, name is Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione. This compound has unique chemical properties. The synthetic route is as follows. HPLC of Formula: C10H6N2O3

In a 1000 mL round flask, a mixture of Compound B-1 (49.4 g, 0.24 mol) and phosphorus oxychloride (720 mL) was stirred at reflux for 7.5 h 7. The reaction mixture is cooled to room temperature and poured into ice water with vigorous stirring to precipitate the precipitate.Generated. The reaction obtained therefrom was filtered to give Compound B (45.1 g, 77% yield, white solid).

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 62208-68-8, Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione.

Reference:
Patent; LG Chem, Ltd.; Han Su-jin; Lee Jeong-ha; Lee Dong-hun; Jang Bun-jae; Jeong Min-u; Park Seul-chan; (56 pag.)KR2019/113662; (2019); A;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Extended knowledge of Benzofuro[3,2-d]pyrimidine-2,4(1H,3H)-dione

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,62208-68-8, its application will become more common.

Electric Literature of 62208-68-8, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 62208-68-8 as follows.

Intermediate I-3 (20 g, 98.9 mmol)Dissolve in a 500 mL round bottom flask with 300 mL of phosphorus oxychloride.Cool down to -30 C,N,N-Diisopropylethylamine (25.6 g, 0.2 mol) was added slowly.The mixture was stirred under reflux for 36 hours, and then cooled to room temperature.The reaction solution was poured into ice water and extracted with ethyl acetate.The extracted organic phase is washed with a saturated sodium hydrogen carbonate solution.And remove water with sodium sulfate.The treated organic phase was concentrated to dryness to give Intermediate I-4 (10.6 g, 45%).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,62208-68-8, its application will become more common.

Reference:
Patent; Zhejiang Huaxian Optoelectric Technology Co., Ltd.; Zheng Xianzhe; Huang Dong; Hua Wanming; Quan Meizi; Zhao Xiaoyu; (34 pag.)CN109678868; (2019); A;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia