Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070018Generated: November 2, 2026

Sodium hydride → 1-benzyloxymethyl-4-chloro-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/2070018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzyl chloromethyl etherHCID 137983—
Reactant4-Chloro-1H-pyrazolo[3,4-b]pyridineHCID 310045—
SolventDimethylformamideHCID 6228—
Product1-benzyloxymethyl-4-chloro-1H-pyrazolo[3,4-b]pyridineHCID 5939854458.3%

Reaction Steps

4-Chloro-1H-pyrazolo[3,4-b]pyridine (371 mg, 2.42 mmol) was dissolved in anhydrous DMF (1 mL), and sodium hydride (60%, 116 mg, 2.42 mmol) was added thereto. The resulting mixture was stirred under ice-cooling for 30 minutes, and then benzyloxymethyl chloride (0.48 mL, 3.39 mmol) was added thereto. The resulting mixture was stirred under ice-cooling for 1 hour and concentrated under reduced pressure. The residue was partitioned between ethyl acetate (80 mL) and saturated brine (20 mL). The aqueous layer was further extracted with ethyl acetate (70 mL). The combined organic layer was washed with saturated brine, dried, and concentrated. The residue was purified by silica-gel column chromatography (Fuji Silysia, BW300, 70 g, n-hexane:EtOAc=5:1) to give 1-benzyloxymethyl-4-chloro-1H-pyrazolo[3,4-b]pyridine as a light-yellow syrup (386 mg, yield: 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299252B2
Source datasetuspto-grants-2012_10
ORD IDord-f274fe4a7493471883e4e9e99d91dac9
Source noteuspto-grants-2012_10