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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222250Generated: October 30, 2026

Ethanol → tert-butyl 4-(3-phenyl-1H-pyrazol-5-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/222250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactanttert-Butyl 4-(3-oxo-3-phenylpropanoyl)piperidine-1-carboxylateHCID 49760127—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 4-(3-phenyl-1H-pyrazol-5-yl)piperidine-1-carboxylateHCID 67109296—

Reaction Steps

A mixture of tert-butyl 4-(3-oxo-3-phenylpropanoyl)piperidine-1-carboxylate (3.1 g), hydrazine monohydrate (0.5 mL), ethanol (30 mL), and THF (30 mL) was stirred at room temperature for about 15 hours, and at 60° C. for 1 hour. Hydrazine monohydrate (0.5 mL) was further added thereto, followed by stirring again at 60° C. for 3 hours. Hydrazine monohydrate (4.0 mL) was added thereto again, followed by stirring at 60° C. for 8 hours. After leaving to be cooled, the solvent was evaporated under reduced pressure, and to the residue were added diisopropyl ether and methanol, followed by stirring. The resulting solid was collected by filtration and dried under reduced pressure to obtain tert-butyl 4-(3-phenyl-1H-pyrazol-5-yl)piperidine-1-carboxylate (2.46 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207199B2
Source datasetuspto-grants-2012_06
ORD IDord-4edd8abd079f425ab29f50450bbf513d
Source noteuspto-grants-2012_06