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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8293Generated: October 24, 2026

Water → 4-(2-Furyl)-1-(3-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine

https://huagongshe.com/en/reaction/8293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantBenzene, 1-(bromomethyl)-3-nitro-HCID 77568—
Reactant4-(2-Furyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amineHCID 22015500—
SolventDimethylformamideHCID 6228—
Product4-(2-Furyl)-1-(3-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amineHCID 2201548947%

Reaction Steps

A solution of 4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine (603 mg, 3 mmol) in DMF (3 mL) at 0° C. was treated with NaH (120 mg, 60%, 3 mmol), stirred for 20 min, treated with 3-nitrobenzyl bromide (648 mg, 3 mmol), stirred at room temperature for 1 h, poured into water, extracted with EtOAc, dried (MgSO4) and concentrated in vacuo. The crude product was purified by chromatography EtOAc:Heptane, 1:1) to give the title compound as a cream solid (472 mg, 47%). A portion of the solid (70 mg) was suspended in MeOH, treated with HCl in dioxan (4-M, 1 mL), diluted with diethyl ether and filtered to give the hydrochloride salt of the title compound (79 mg, 100%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087754B2
Source datasetuspto-grants-2006_08
ORD IDord-d3565e498df14ed8bae23550cb576b19
Source noteuspto-grants-2006_08