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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole | HCID 11368884 | — |
| Reactant | tert-Butyl aziridine-1-carboxylate | HCID 15933185 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18407256 | HCID 18407256 | 34.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476060B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-2be5056a349d4cfbaba3a020fcc6b36b |
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| Source note | uspto-grants-2002_11 |
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