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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169705Generated: November 3, 2026

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

https://huagongshe.com/reaction/1169705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-IodopyrazoleHCID 77022—
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(4-iodo-1H-pyrazol-1-yl)piperidine-1-carboxylateHCID 4548038966%

Reaction Conditions

Temperature4 °C

Reaction Steps

NaH (1.2 eq., 0.68 mmol) was added portionwise to a stirred solution of 4-iodopyrazole (0.57 mmol) in DMF (2 L) at 4° C. The resulting mixture was stirred for 1 hour at 4° C. and 4-methanesulfonyloxy-piperidine-1-carboxylic acid tert-butyl ester, compound 2 (1.1 eq., 0.63 mmol) was then added. The resulting mixture was heated to 100° C. for 12 h. The reaction was quenched with H2O and extracted with EtOAc several times. The combined organic layers were dried, filtered, and concentrated to afford an orange oil. The residue was purified by silica gel chromatography (eluting with 5% EtOAc in pentane) to give compound 3 as a white solid (140 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825137B2
Source datasetuspto-grants-2010_11
ORD IDord-fa3250c10c324601b4f01633541acef7
Source noteuspto-grants-2010_11