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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446920Generated: October 30, 2026

Methyl iodide → 4-bromo-1-(2-methoxy-ethyl)-1H-pyrazolo[3,4-c]pyridine

https://huagongshe.com/reaction/446920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-Bromo-pyrazolo[3,4-c]pyridin-1-yl)-ethanolHCID 57606782—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-1-(2-methoxy-ethyl)-1H-pyrazolo[3,4-c]pyridineHCID 57606794—

Reaction Steps

A solution of 675 mg of 2-(4-bromo-pyrazolo[3,4-c]pyridin-1-yl)-ethanol (Intermediate 2.2; 2.79 mmol, 1 eq.) in 33 mL THF was treated at rt with 183 mg sodium hydride (55-60% suspension; 4.18 mmol, 1.5 eq.) and stirred for 30 min upon which 0.194 mL methyl iodide (3.07 mmol, 1.1 eq.) were added and stirring was continued for 2 h. The reaction mixture was quenched with water, extracted with ethyl acetate, the combined organic layers were dried and concentrated in vacuo. Flash column chromatography provided 500 mg of the corresponding methyl ether target compound (1.95 mmol, 70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481539B2
Source datasetuspto-grants-2013_07
ORD IDord-247867cd1dc9431bb7183698468bf6dd
Source noteuspto-grants-2013_07