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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059999Generated: October 30, 2026

Hydrochloric Acid → HCID 178477471, compound

https://huagongshe.com/reaction/1059999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantN-(3-(4-methoxypyridin-2-yl)phenyl)thioureaHCID 18667488—
SolventDimethylformamideHCID 6228—
SolventIodoethaneHCID 6340—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178477471HCID 178477471—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of N-(3-(4-methoxypyridin-2-yl)phenyl)thiourea (171 mg) in N,N-dimethylformamide (4 ml) were added a solution of hydrogen chloride in 1,4-dioxane (4N, 0.33 ml) and iodoethane (0.263 ml), and the mixture was stirred at 50° C. for 1.5 hours. Ethyl acetate (100 ml) was added to the mixture, and the mixture was cooled. The precipitate was collected by filtration. The precipitate was dissolved in water, and to the solution was added a saturated aqueous sodium hydrogencarbonate solution and extracted with dichloromethane. The organic layer was washed with brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was dissolved in ethyl acetate, and to the solution was added a solution of hydrogen chloride in 1,4-dioxane (4N, 0.5 ml). The precipitate was collected by filtration and dried under reduced pressure to give N-(3-(4-methoxypyridin-2-yl)phenyl)-S-ethylisothiourea dihydrochloride (204 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-9834db2496c547e68a2e30b6753caea6
Source noteuspto-grants-2003_02