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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573235Generated: October 25, 2026

Trityl chloride → 3-(6-bromopyridin-2-yl)-1-trityl-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/573235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178419383HCID 178419383—
SolventDimethylformamideHCID 6228—
Product3-(6-bromopyridin-2-yl)-1-trityl-1H-pyrazolo[3,4-b]pyridineHCID 86665933—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred suspension of 3-(6-bromo-2-pyridyl)-1H-pyrazolo[5,4-b]pyridine (3.00 g, 10.90 mmol) in dry DMF (30.00 mL) was cooled in an ice-bath. Sodium hydride (479.6 mg, 11.99 mmol) was added in one portion and the resulting mixture changed to a yellow solution and was stirred at 0° C. for 30 minutes. Trityl chloride (3.189 g, 11.44 mmol) was added in one portion and the resulting yellow suspension was stirred at RT for 60 minutes, by which time it was a bright yellow suspension. Analysis by LCMS showed presence of desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029546B2
Source datasetuspto-grants-2015_05
ORD IDord-1fa049f610504a89af08e10c486af461
Source noteuspto-grants-2015_05