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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262481Generated: October 27, 2026

Sodium hydride → HCID 42633816, compound

https://huagongshe.com/reaction/2262481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(S)-(1,4-Dimethylpiperazin-2-YL)methanolHCID 7035990—
Reactant4-Nitrophenyl 4-phenylpiperazine-1-carboxylateHCID 59594481—
SolventTetrahydrofuranHCID 8028—
ProductHCID 42633816HCID 4263381636.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,4-dimethyl-(S)-2-hydroxymethyl piperazine (Intermediate 3; 1.49 g, 10.3 mmol) in THF (20 mL) at 0° C. was added sodium hydride (1.24 g, 60% dispersion in mineral oil, 31.0 mmol). The reaction mixture was stirred for several minutes at 0° C. and then 4-nitrophenyl 4-phenylpiperazine-1-carboxylate (Intermediate 2; 3.72 g, 11.4 mmol) in THF (20 mL). The reaction mixture was allowed to warm to room temperature and stirred for 7 hours. The reaction mixture was then cooled to 0° C. and quenched with the drop-wise addition of sat aq NaHCO3 solution. The THF was removed in vacuo, the aqueous phase extracted with EtOAc (×3), combined organic phases washed with sat aq NaHCO3 solution (×6), dried (MgSO4) and concentrated in vacuo. The residue was suspended in water: formic acid solution [1:1] (20 mL), filtered and the filtrate was purified by reverse phase column chromatography (gradient eluting with methanol in water, with 1% formic acid in each solvent, 0-15%). The resulting residue was dissolved in DCM (50 mL) and stirred with solid K2CO3 for 20 minutes, filtered and concentrated in vacuo to give [(2S)-1,4-dimethylpiperazin-2-yl]methyl 4-phenylpiperazine-1-carboxylate (1.25 g, 36%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851471B2
Source datasetuspto-grants-2010_12
ORD IDord-ccff4d17c97a437a890330a348de7e1a
Source noteuspto-grants-2010_12