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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530604Generated: November 2, 2026

N-bromobutanimide → tert-Butyl 3-(4-bromo-1-methyl-1H-pyrazol-5-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1530604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactanttert-butyl 3-(1-methyl-1H-pyrazol-5-yl)piperidine-1-carboxylateHCID 68313066—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-(4-bromo-1-methyl-1H-pyrazol-5-yl)piperidine-1-carboxylateHCID 68313245—

Reaction Steps

To a solution of tert-butyl 3-(1-methyl-1H-pyrazol-5-yl)piperidine-1-carboxylate (680 mg, 2.50 mmol) in THF (20 mL) was added NBS (486 mg, 2.80 mmol). The reaction mixture was stirred for 2 h. After concentration, the residue was purified by silica gel chromatography eluting with a 0-50% gradient of EtOAc in petroleum ether to give tert-butyl

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-def8965d9181484ebd0f93846268d550
Source noteuspto-grants-2015_07