Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016607Generated: October 28, 2026

3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole → HCID 18407256, compound

https://huagongshe.com/reaction/1016607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazoleHCID 11368884—
Reactanttert-Butyl aziridine-1-carboxylateHCID 15933185—
SolventTolueneHCID 1140—
ProductHCID 18407256HCID 1840725634.1%

Reaction Steps

Part A: A stirred solution of 3-(4-chlorophenyl)-4,5-dihydro-4-phenyl-1H-pyrazole (5.00 gram, 19.5 mmol) and N-(tert-butoxycarbonyl)aziridine (2.00 gram, 14.0 mmol) in toluene (100 ml) was heated at reflux temperature for 16 hours. After concentration in vacuo the residue was purified by flash chromatography (petroleum ether/diethyl ether=3/1 (v/v)), followed by petroleum ether/diethyl ether=1/1 (v/v)). After concentration in vacuo the remaining oily residue was crystallised from diisopropyl ether to afford 1-[2-((tert-butoxycarbonyl)amino)ethyl]-3-(4-chlorophenyl)-4,5-dihydro-4-phenyl-1H-pyrazole (1.91 gram, 34%). Repeated crystallisations from the mother liquor afforded an additional amount of crystalline 1-[2-((tert-butoxycarbonyl)amino)ethyl]-3-(4-chlorophenyl)-4,5-dihydro-4-phenyl-1H-pyrazole (1.19 gram).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476060B2
Source datasetuspto-grants-2002_11
ORD IDord-2be5056a349d4cfbaba3a020fcc6b36b
Source noteuspto-grants-2002_11