HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059999Generated: October 30, 2026
Hydrochloric Acid → HCID 178477471, compound
https://huagongshe.com/reaction/1059999
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-(3-(4-methoxypyridin-2-yl)phenyl)thiourea | HCID 18667488 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Iodoethane | HCID 6340 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178477471 | HCID 178477471 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521643B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-9834db2496c547e68a2e30b6753caea6 |
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| Source note | uspto-grants-2003_02 |
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