Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528753Generated: October 26, 2026

Pyrazole → 3-Pyrazol-1-ylmethyl-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/528753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-((methanesulfonyloxy)methyl)azetidine-1-carboxylateHCID 21959416—
SolventTetrahydrofuranHCID 8028—
Product3-Pyrazol-1-ylmethyl-azetidine-1-carboxylic acid tert-butyl esterHCID 67979283—

Reaction Steps

To 17.9 mg (0.26 mmol) pyrazole in 2 mL dry THF at 0° C. was added 14 mg (0.35 mmol, 60% dispersion in mineral oil) NaH and the reaction was stirred for 30 minutes. 50 mg (0.17 mmol) 3-methanesulfonyloxymethyl-azetidine-1-carboxylic acid tert-butyl ester in 1 mL dry THF was added dropwise and the reaction was allowed to warm to room temperature for 16 hours. The solvent was evaporated and the remaining residue was partitioned between 25 mL H2O and 25 mL EtOAc. The organic phase was washed with 25 mL 1% citric acid solution, H2O (3×25 mL), 25 mL brine and dried with Na2SO4. After filtration and evaporation of the solvent the product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-ac768b0553a24003b73c7895ccfea3d7
Source noteuspto-grants-2016_05