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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892989Generated: October 29, 2026

Potassium Carbonate → HCID 22418808, compound

https://huagongshe.com/reaction/892989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonateHCID 85257—
Reactant4-(Piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidineHCID 14585243—
SolventAcetonitrileHCID 6342—
ProductHCID 22418808HCID 22418808—

Reaction Steps

The N-protected 2-hydroxyethylpiperazine (3.0 g), triethylamine (1.42 g) and methylene chloride (30 ml) is cooled to 0° in an ice bath under nitrogen. A mixture of methanesulfonyl chloride (1.64 g) in methylene chloride (30 ml) is added dropwise over 10 min. The cooling bath is removed and the mixture allowed to warm to 20°-25° for 30 min. The mixture is then washed with water (60 ml), dried over sodium sulfate and the solvent removed to give crude mesylate. 4-[2,6-Bis(1-pyrrolidinyl)-4-pyrimidinyl]piperazine (4.23 g), potassium carbonate (1.93 g) and acetonitrile (150 ml) are added to the crude mesylate. The mixture is heated at reflux for 18 hr. The acetonitrile is removed under reduced pressure and the residue distributed between chloroform (200 ml) and water (200 ml). The phases are separated, the organic phase is washed with saline, dried over sodium sulfate and the solvent removed under reduced pressure to give an oil. The oil is flash chromatographed on silica gel (200 g) with ethyl acetate/methanol/ammonium hydroxide (9.5/0.4/0.1). The appropriate fractions are pooled and concentrated to give the N-protected form of the title compound as a solid, mp 148°-149°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120843
Source datasetuspto-grants-1992_06
ORD IDord-6e1590ab3bdb4e11a5e0613b63097f0a
Source noteuspto-grants-1992_06