Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636282Generated: October 29, 2026

Potassium Iodide → 1-pyrimidin-2-yl-1,4-diazepane

https://huagongshe.com/reaction/1636282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantHexahydro-1,4-diazepineHCID 68163—
Reactant2-ChloropyrimidineHCID 74404—
SolventAcetonitrileHCID 6342—
Product1-pyrimidin-2-yl-1,4-diazepaneHCID 277240948%

Reaction Steps

50 ml of acetonitrile was added to 10.0 g (0.1 mole) of homopiperazine, 2.9 g (0.025 mole) of 2-chloropyrimidine, 6.9 g (0.05 mole) of potassium carbonate and a catalytic amount of potassium iodide, and the mixture was refluxed under heating for 11 hours. The mixture was cooled to room temperature and then filtered, the filtrate obtained was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (eluent; a chloroform:methanol=8:2 mixed solution) to obtain 2.14 g of 1-(2-pyrimidyl)homopiperazine as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034086
Source datasetuspto-grants-2000_03
ORD IDord-dd1f95b2fd884e55b18f349aa1d75c39
Source noteuspto-grants-2000_03