Some scientific research about 3-Bromo-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,54738-73-7, its application will become more common.

Synthetic Route of 54738-73-7 ,Some common heterocyclic compound, 54738-73-7, molecular formula is C5H3BrN4O, its 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.

3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-ol (Intermediate A) (15.08 g, 70.5 mmol) was suspended in 189 ml of phosphous oxychloride. Diethylaniline (19 ml, 119.4 mmol) was added and the resulting reaction mixture was heated to 106 C. for 2 hours. After cooling to room temperature, the solvent was removed and the resulting amber syrup was poured to 300 ml of ice-water. 20 minutes later, the aqueous layer was extracted with diethyl ether (500 ml*4). The combined organic layer was washed, dried and evaporated to give 6.87 g of 3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine as light yellow solid. 1H NMR (DMSO) 8.857 (s 1H), 14.84 (bs, 1H); LC/MS (MH+=233).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,54738-73-7, its application will become more common.

Reference:
Patent; Abbott Laboratories; US6921763; (2005); B2;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia