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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051589Generated: November 2, 2026

Ethyl Acetate → tert-butyl 4-(3-bromo-1H-pyrazol-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1051589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
ReactantHCID 178419412HCID 178419412—
SolventDimethylformamideHCID 6228—
Producttert-butyl 4-(3-bromo-1H-pyrazol-1-yl)piperidine-1-carboxylateHCID 6852309525.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 4-(methylsulfonyloxy)piperidine-1-carboxylate (0.837 g, 3.00 mmol), 3-bromo-1H-pyrazole (0.441 g, 3.02 mmol), and cesium carbonate (2.94 g, 9.02 mmol) in DMF (10 mL) stirred for 5 h at 100° C. The reaction mixture was cooled to room temperature and poured ethyl acetate (50 mL). The mixture was washed with water (3×10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue purified via column chromatography on silica gel (eluting with 10% dichloromethane/methanol to afford tert-butyl 4-(3-bromo-1H-pyrazol-1-yl)piperidine-1-carboxylate (0.25 g, 25%) as a white solid. MS (ESI, pos. ion) m/z 330, 332 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388161B2
Source datasetuspto-grants-2016_07
ORD IDord-e68a9a2de8414e60ade7b64ba037f6da
Source noteuspto-grants-2016_07