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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581638Generated: October 26, 2026

Sodium hydride → 4-Cyclopropylmethyl-3-oxopiperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1581638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBromomethylcyclopropaneHCID 81503—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product4-Cyclopropylmethyl-3-oxopiperazine-1-carboxylic acid tert-butyl esterHCID 67084922100%

Reaction Steps

Sodium hydride (60% dispersion in oil) (0.40 g, 10.0 mmol) was added portionwise over 10 min to a solution of 3-oxopiperazine-1-carboxylic acid tert-butyl ester (1.00 g, 5.0 mmol) in N,N-dimethylacetamide (10 ml). The mixture was stirred for 30 min before addition of bromomethylcyclopropane (1.45 ml, 15.0 mmol) and then stirred for a further 18 h. The mixture was diluted with water (100 ml) and extracted with EtOAc (2×100 ml). The combined organic extracts were washed with brine (50 ml), dried over MgSO4 and evaporated to give 4-cyclopropylmethyl-3-oxopiperazine-1-carboxylic acid tert-butyl ester (1.27 g, 100%) as a yellow oil. This oil was dissolved in dichloromethane and hydrogen chloride bubbled through the reaction (2×10 min). The solvent was evaporated to give 1-cyclopropylmethylpiperazin-2-one.HCl (0.95 g, 100%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730681B2
Source datasetuspto-grants-2004_05
ORD IDord-34c71b5d338a4d57899b9c485c117888
Source noteuspto-grants-2004_05