HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263262Generated: October 25, 2026
Hydrochloric Acid → 1-[4-(2,3-Difluorophenyl)-1,3-thiazol-2-yl]piperazine hydrochloride
https://huagongshe.com/reaction/2263262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tert-butyl 4-[4-(2,3-difluorophenyl)-1,3-thiazol-2-yl]piperazine-1-carboxylate | HCID 68781293 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[4-(2,3-Difluorophenyl)-1,3-thiazol-2-yl]piperazine hydrochloride | HCID 68776288 | — |
Reaction Steps
A 4 N solution (50 ml) of hydrogen chloride in ethyl acetate was added to a solution of tert-butyl 4-[4-(2,3-difluorophenyl)-1,3-thiazol-2-yl]piperazine-1-carboxylate (4.20 g, 11.0 mmol) in ethyl acetate (100 ml), and the mixture was stirred at room temperature for 14 hours. Hexane was added to the reaction mixture, and crystals were collected by filtration to give 1-[4-(2,3-difluorophenyl)-1,3-thiazol-2-yl]piperazine hydrochloride. The hydrochloride was dissolved in water, neutralized with a 1 N sodium hydroxide aqueous solution, and extracted with chloroform. The extract was washed with water, and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to give 1.76 g (56.8%) of the desired product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851473B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-dc32fcfb544e4a39b5e700b7d2f522cf |
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| Source note | uspto-grants-2010_12 |
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