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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648490Generated: October 30, 2026

Sodium Iodide → HCID 15293733, compound

https://huagongshe.com/reaction/1648490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidineHCID 14585243—
ReactantHCID 15293732HCID 15293732—
SolventAcetonitrileHCID 6342—
ProductHCID 15293733HCID 15293733—

Reaction Steps

4-(3-Chloropropoxy)indole-2-carboxamide (0.44 g), 4-(1-piperazinyl)-2,6-di-1-pyrrolidinylpyrimidine (0.525 g), powdered potassium carbonate (0.12 g) and sodium iodide (0.075 g) are combined in acetonitrile (50 ml) and heated at reflux for 96 hr. Although TLC showed both starting material and product remained in the reaction mixture, the mixture was concentrated under reduced pressure and the residue partitioned between 1N potassium bicarbonate and methylene chloride. The layers are separated, the aqueous layer is extracted with methylene chloride, the pooled organic extract is washed with water, then saline, dried over magnesium sulfate and concentrated. The residue is chromatographed over silica gel (250 ml) and eluted with methanol/methylene chloride (3.5/96.5). The appropriate fractions are pooled and concentrated. Crystallization from acetonitrile gives the title compound, mp 151°-2° (foam); the proposed structure is supported by NMR, IR and mass spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436337
Source datasetuspto-grants-1995_07
ORD IDord-7b3322ffb51446ea9b3ad63852ba1155
Source noteuspto-grants-1995_07