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5413-96-7

4-chloro-1,6-dimethyl-1H-pyrazolo[3,4-d]pyrimidine synthesis

4synthesis methods
-

Yield:5413-96-7 85%

Reaction Conditions:

with ammonium hydroxide in tetrahydrofuran at 25; for 24 h;

Steps:

2 Step2: Amination

To a suspension of 4,6-Dichloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidine (2.84g, 14 mmol) in the reaction flask and then add THF(56ml) to wait for the solid to dissolve completely. Then add 20g 30% ammonium solution and react at room temperature (25 °C) for 24h and poured 60ml water into the solution, filtration by suction to afford the 6-chloro-1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine (2.17g, 85%) as a yellow solid powder.

References:

WO2021/80980,2021,A1 Location in patent:Page/Page column 20