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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522596Generated: October 31, 2026

Methyl iodide → 2H-Pyrazolo[4,3-b]pyridine, 7-bromo-2-methyl-

https://huagongshe.com/reaction/1522596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant7-Bromo-1H-pyrazolo[4,3-b]pyridineHCID 67470457—
SolventTetrahydrofuranHCID 8028—
Product2H-Pyrazolo[4,3-b]pyridine, 7-bromo-2-methyl-HCID 67469527—

Reaction Steps

A solution of 7-bromo-1H-pyrazolo[4,3-b]pyridine (100 mg, 0.505 mmol) and sodium hydride (24.24 mg, 0.606 mmol) in THF (2.0 mL) was stirred at 0° C. for 15 minutes. Iodomethane (71.7 mg, 0.505 mmol) was added, and the reaction was warmed to room temperature for 1 hour. The reaction was quenched with water, extracted with EtOAc, dried over MgSO4, and evaporated to dryness to give 7-bromo-2-methyl-2H-pyrazolo[4,3-b]pyridine which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073918B2
Source datasetuspto-grants-2015_07
ORD IDord-c8af38c32b404e4aac0eaf59cf76df9d
Source noteuspto-grants-2015_07