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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571375Generated: October 31, 2026

Trityl chloride → 6-chloro-3-(4-fluorophenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/571375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
Reactant6-Chloro-3-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridineHCID 76847165—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-chloro-3-(4-fluorophenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 8952582682.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Chloro-3-(4-fluorophenyl)-1H-pyrazolo[4,3-c]pyridine (1 g, 4.04 mmol) was dissolved in DMF (20 mL) and cooled to 0° C. Sodium hydride (0.242 g, 6.06 mmol) was then added and the reaction mixture stirred for one hour. Trityl chloride (1.351 g, 4.85 mmol) was then added and the reaction mixture warmed to room temperature and stirred for 1.5 hours. The reaction mixture was diluted with water and stirred at 0° C. for one hour to promote perception. The solid was filtered and rinsed with water. The solid was diluted with DCM and concentrated in vacuo while loading onto silica gel. The residue was purified by flash chromatography (2-30% EtOAc/isohexane) to give 6-chloro-3-(4-fluorophenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridine (1.63 g, 3.33 mmol, 82%). MS ESI calc'd. For C31H21ClFN3 [M+1]+ 490, found 490.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023865B2
Source datasetuspto-grants-2015_05
ORD IDord-d2a6f09b87d14c51a78e53043bce8278
Source noteuspto-grants-2015_05