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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268157Generated: November 1, 2026

Hydrochloric Acid → HCID 20581788, compound

https://huagongshe.com/reaction/1268157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthanimidic acid, ethyl ester, hydrochloride (1:1)HCID 2724290—
ReactantHCID 20581786HCID 20581786—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20581788HCID 20581788104.1%

Reaction Steps

To a solution of N-[3-(3-amidinophenyl)-2-methyl-2-(E)-propenyl]-N-[4-(piperidin-4-yloxy)phenyl]ethanesulfonamide dihydrochloride (303 mg) in ethanol (10 ml) were added ethyl acetimidate hydrochloride (246 mg) and triethylamine (0.460 ml). The resulting mixture was stirred at room temperature for 12 hours. After addition of a 4M solution of hydrogen chloride in dioxane (0.9 ml), the resulting mixture was concentrated in vacuo. The residue was purified by preparative HPLC (YMC-Pack ODS YMC) using 20% aqueous acetonitrile as an eluant to afford an amorphous solid. To a solution of the solid in methanol (10 ml) was added a 4M solution of hydrogen chloride in dioxane (0.4 ml) and the mixture was concentrated to dryness in vacuo. The resulting amorphous solid was dissolved in water (10 ml) and the solution was lyophilized to give the title compound (170 mg, yield 45%) as a colorless amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-47cc6c356e9c488f9fef0f81cfbe9320
Source noteuspto-grants-2003_04