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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349532Generated: November 1, 2026

Trityl chloride → 5-Amino-1-[2-(trityloxy)ethyl]pyrazole-4-carbonitrile

https://huagongshe.com/reaction/349532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbonitrileHCID 219852—
SolventPyridineHCID 1049—
Product5-Amino-1-[2-(trityloxy)ethyl]pyrazole-4-carbonitrileHCID 1796201898%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 5-amino-1-(2-hydroxyethyl)pyrazole-4-carbonitrile (10 g, 65.7 mmol) and pyridine (100 ml) was added triphenylmethyl chloride (22.3 g, 78.9 mmol) at room temperature. After stirring at 60° C. for 6 hours, the reaction mixture was concentrated in vacuo. To the residue were added tetrahydrofuran and brine, and the separated organic layer was washed with brine. The extract was dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was triturated with ethyl acetate to give 5-amino-1-[2-(trityloxy)ethyl]pyrazole-4-carbonitrile (25.4 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179801B2
Source datasetuspto-grants-2007_02
ORD IDord-968dc57983c84bc1a06f349e3c975ef6
Source noteuspto-grants-2007_02