HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059988Generated: November 2, 2026
Hydrochloric Acid → HCID 178477470, compound
https://huagongshe.com/reaction/1059988
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-(3-(4-methylpyridin-2-yl)phenyl)thiourea | HCID 18667523 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Iodoethane | HCID 6340 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178477470 | HCID 178477470 | — |
Reaction Steps
To a suspension of N-(3-(4-methylpyridin-2-yl)phenyl)thiourea (243 mg) in N,N-dimethylformamide (5 ml) were added a solution of hydrogen chloride in 1,4-dioxane (4N, 0.5 ml) and iodoethane (0.4 ml), and the mixture was stirred at 50° C. for 2 hours. Ethyl acetate (100 ml) was added to the mixture, and the mixture was cooled. The precipitate was collected by filtration and dissolved in water. To the solution was added a saturated aqueous sodium hydrogencarbonate solution, and the mixture was 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, 1 ml). The precipitate was collected by filtration and dried under reduced pressure to give N-(3-(4-methylpyridin-2-yl)phenyl)-S-ethylisothiourea dihydrochloride (294 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-3847f95dc2e8444592e1d7e248d0ec9e |
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| Source note | uspto-grants-2003_02 |
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