HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392944Generated: October 27, 2026
Hydrochloric Acid → 2-[4-(4-Trifluoromethyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamide
https://huagongshe.com/reaction/1392944
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-[4-(4-Trifluoromethyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid methyl ester | HCID 69201003 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[4-(4-Trifluoromethyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamide | HCID 11487392 | 16% |
Reaction Steps
To a solution of compound 12f (125 mg, 0.287 mmol) in 1,4-dioxane (2 mL) were added hydroxylamine hydrochloride (199 mg, 2.87 mmol) and a freshly prepared solution of sodium methoxide in methanol (99 mg, 4.30 mmol of sodium dissolved in 1 mL of methanol) under a N2 atmosphere. The reaction mixture was stirred at room temperature for 2 h. The reaction mixture was acidified to pH˜6 with 1M HCl and the formed precipitates were filtered off. The filtrate was diluted with ethyl acetate (5 mL) and water (2 mL) and the organic layer was separated. The aqueous layer was washed with ethyl acetate (5 mL) and the combined organic layers were dried on sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC to give 13f (20 mg, yield 16%). HPLC 85.42% (Rt=14.11 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07345043B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-0923a78cb4a84819bcb4b5b38f5b2f5f |
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| Source note | uspto-grants-2008_03 |
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