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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930569Generated: October 31, 2026

Ethyl Acetate → Ethyl [3-(bromomethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl]acetate

https://huagongshe.com/reaction/930569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 67103879HCID 67103879—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl [3-(bromomethyl)-1H-pyrazolo[3,4-b]pyridin-1-yl]acetateHCID 57642772—

Reaction Steps

A mixture of (3-methyl-pyrazolo[3,4-b]pyridine-1-yl)ethyl acetate (2.5 mmol, 1 eq.), NBS (3.0 mmol, 1.2 eq.), and benzoly peroxide (0.05 mmol, 0.02 eq.) in 10 mL of CCl4 was refluxed for 1.5 h. The resultant mixture was cooled to rt, and diluted with 500 mL of EtOAc. The resultant solution was then washed with 100 mL of sat. sodium bicarbonate aqueous solution, brine solution, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude residue was purified by silica gel chromatography (20% EtOAc in hexane to 35% EtOAc in hexane) to provide 450.2 mg of the desired product: HPLC retention time=2.50 minutes (Agilent Zorbax SB-C18, 2.1×50 mm, 5μ, 35° C.) using 1 ml/min flow rate, a 2.5 minute gradient of 0% to 100% B with a 1.1 minute wash at 100% B (A=0.1% formic acid/5% acetonitrile/94.9% water, B=0.1% formic acid/5% water/94.9% acetonitrile); MS (ES) M+H expect=298.0. found=298.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296740B2
Source datasetuspto-grants-2016_03
ORD IDord-41d9fd7bf61942b3bcf91cf092a73efd
Source noteuspto-grants-2016_03