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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493695Generated: October 25, 2026

Hydrochloric Acid → HCID 178482540, compound

https://huagongshe.com/reaction/493695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-((6-Chloro-2-naphthyl)sulfonyl)propionyl)piperazineHCID 23130883—
ReactantHCID 178482537HCID 178482537—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178482540HCID 178482540121.4%

Reaction Steps

A suspension of 1-(3-((6-chloro-2-naphthyl)sulfonyl)propionyl)piperazine (2.5 g) obtained in Example 3a), N-((2Z)-4-chloromethyl-3-methyl-1,3-thiazol-2(3H)-ylidene)-N-methylamine hydrochloride (2.2 g) and potassium carbonate (2.4 g) in DMF (50 mL) was mixed at 65° C. for 3 hours. The solvent was distilled off under reduced pressure, the residue was diluted with an aqueous potassium carbonate solution, and extracted with chloroform. The extract was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The product, which was obtained by the purification of the residue with a basic silica gel column, was dissolved in ethyl acetate. A solution of hydrogen chloride in ether was added thereto, and the mixture was concentrated and dried to give the title compound (2.4 g) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534887B2
Source datasetuspto-grants-2009_05
ORD IDord-3a3fbf0254c84df7ae80a04ae775c56e
Source noteuspto-grants-2009_05