Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650890Generated: October 27, 2026

Water → 1-(imidazolin-2-yl)-4-Boc-piperazine

https://huagongshe.com/reaction/650890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4,5-dihydro-1H-imidazole-2-sulfonic acidHCID 274561—
SolventMethanolHCID 887—
Product1-(imidazolin-2-yl)-4-Boc-piperazineHCID 18424132—

Reaction Steps

1.86 of Boc-piperazine were combined with 25 ml of water, 25 ml of methanol, 2.77 g of K2CO3 and 1.5 g of imidazoline-2-sulphonic acid and stirred for 2 days at RT. After dilution with water the mixture was extracted with EE and chromatographed over silica gel. 0.8 g of 1-(imidazolin-2-yl)-4-Boc-piperazine were obtained. This substance was combined with 6.2 ml of DMF and 136 mg of NaH dispersion (60%). After one hour, 0.214 ml of methyl iodide was added dropwise and the reaction mixture was left for three days at RT. It was combined with water, extracted with EE and chromatographed over silica gel. In this way, 0.47 g of 1-(1-methylimidazolin-2-yl)-4-Boc -piperazine was obtained, which was treated with 5 ml of 4N HCl in dioxane at RT. After one hour, the mixture was concentrated by evaporation, stirred with ether and evaporated to dryness in vacuo. 0.38 g of 1-(1-methyl -imidazolin-2-yl)-piperazine dihydrochloride was thus obtained as a solid substance (yield 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277840B1
Source datasetuspto-grants-2001_08
ORD IDord-780b163fe0994dfc83742ae3532af642
Source noteuspto-grants-2001_08