Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433101Generated: October 31, 2026

Sodium Hydroxide → 4-benzyloxycarbonyl-3-(S)-methoxymethyl-1-[(2-methylthiopyrimidin-5-yl)-methyl]-piperazine-2-one

https://huagongshe.com/reaction/1433101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 60209911HCID 60209911—
Reactant4-Benzyloxycarbonyl-3-(S)-methoxymethyl-piperazine-2-oneHCID 68898261—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-benzyloxycarbonyl-3-(S)-methoxymethyl-1-[(2-methylthiopyrimidin-5-yl)-methyl]-piperazine-2-oneHCID 6890037633%

Reaction Steps

4-Benzyloxycarbonyl-3-(S)-methoxymethyl-piperazine-2-one (0.1 g 0.37 mmol), 5-bromomethyl-2-methylthiopyrimidine (0.08 g, 0.37 mmol) and tetra-n-butylammonium bromide (0.06 g, 0.19 mmol) are placed in dichloromethane (1 mL) and 50% aqueous NaOH (0.03 mL) and stirred for 4 h. The mixture is diluted with water and is extracted with dichloromethane (2×20 mL). The combined organic extracts are dried (MgSO4) and are evaporated. The residue is purified by flash chromatography (silica gel, 98:2 dichloromethane/methanol) to provide the intermediate title compound as a colorless oil (0.05 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-a172bc08fb7d400e8ae0e97920553fde
Source noteuspto-grants-2009_11