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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590768Generated: October 30, 2026

Trityl chloride → 6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/590768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
Reactant6-chloro-3-iodo-1H-pyrazolo[4,3-c]pyridineHCID 178477833—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 89525858—

Reaction Steps

A solution of 6-chloro-3-iodo-1H-pyrazolo[4,3-c]pyridine (1.874 g, 6.71 mmol) in THF (20 mL) was treated with NaH (60% in mineral oil; 0.402 g, 10.06 mmol) at 0° C. and the mixture was stirred for 50 min. Trityl chloride (2.244 g, 8.05 mmol) was added at 0° C. and the mixture was stirred for 16 h at room temperature, quenched with saturated NH4Cl, and extracted with EtOAc. The organic phase was washed with water, brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified via flash chromatography (0-10% EtOAc-hexanes) to yield 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine. MS ESI calc'd. for C25H18ClIN3[M+1]+ 522. found 522.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-965d577c8faa4636a89d6f1b5642d514
Source noteuspto-grants-2016_01