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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644638Generated: October 31, 2026

Triethylamine → 1-Tert-butyl-3-(4-chlorobenzyl)-1H-pyrazol-5-amine

https://huagongshe.com/reaction/1644638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
Reactant4-(4-Chlorophenyl)-3-oxobutanenitrileHCID 50988847—
SolventEthanolHCID 702—
Product1-Tert-butyl-3-(4-chlorobenzyl)-1H-pyrazol-5-amineHCID 57551173115.6%

Reaction Steps

A solution of 4-(4-chloro-phenyl)-3-oxo-butyronitrile (500 mg, 2 mmol, 1.0 equiv), triethylamine (1.16 mL, 8.3 mmol, 3.2 equiv), and tert-butylhydrazine hydrochloride (1.03 g, 8.3 mmol, 3.2 equiv) in 10 mL of ethanol was heated at 100° C. in a sealed tube. After 4 d, the reaction mixture was cooled to ambient temperature and concentrated in vacuo. The residue was purified via automated flash chromatography (40 g SiO2, gradient from hexanes to ethyl acetate) to afford the product as a yellow oil (610 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124610B2
Source datasetuspto-grants-2012_02
ORD IDord-da5684ac0c8c47309f5c11f334e34c57
Source noteuspto-grants-2012_02