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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590619Generated: October 30, 2026

Sodium hydride → tert-Butyl 4-(4-iodo-1H-pyrazol-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/590619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-IodopyrazoleHCID 77022—
ReactantTert-butyl 4-(methylsulfonyl)piperidine-1-carboxylateHCID 22504298—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(4-iodo-1H-pyrazol-1-yl)piperidine-1-carboxylateHCID 45480389—

Reaction Steps

NaH (60% suspension, 1.13 g, 28.4 mmol) was added portion wise to a solution of 4-iodopyrazole (5 g, 25.7 mmol) in anhydrous DMF (30 mL) at 0° C.; and it was stirred for 1 h. Finally, tert-butyl 4-mesylpiperidine-1-carboxylate (CAS: 141699-59-4) (6.5 g, 32.7 mmol) was added to the reaction mixture and it was stirred at 100° C. for 16 h. It was, then, cooled and quenched with saturated solution of NH4Cl (100 mL). Extraction was carried out using EtOAc (50 mL×2); the combined organic layers were washed with water (100 mL); brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to provide crude product, which was further purified by silica gel column chromatography (20% EtOAc in hexanes) to give title compound Va-1-I (4 g, 41%). LCMS: m/z 378.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233983B2
Source datasetuspto-grants-2016_01
ORD IDord-d08cedf8e3774f68b0ba93e501c60ab2
Source noteuspto-grants-2016_01