HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640044Generated: October 30, 2026
Hydrochloric Acid → HCID 22500834, compound
https://huagongshe.com/reaction/640044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 22500714 | HCID 22500714 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22500834 | HCID 22500834 | 90.8% |
Reaction Steps
4N HCl (5 mL) was added to a stirred solution of N-[1-Boc-4-(hydroxymethyl)piperidin-4-yl]-5-chlorothiophene-2-sulfonamide 5 (0.7 g, 1.7 mmol) in EtOAc (4 mL). The solution was allowed to stir at 25° C. After 30 min, a cloudy solution formed. After 2 h a precipitate formed. TLC (1: 1 EtOAc-hexane) indicated the reaction was complete. The solvent was reduced to ˜2-3 mL, diluted with diethyl ether (6 mL) and filtered through a filter funnel. The precipitate was washed with diethyl ether (3×5 mL) to obtain N-[4-(hydroxymethyl)piperidin-4-yl]-5-chlorothiophene-2-sulfonamide as an amorphous white solid (0.48 g, 90.7%). Mass Spectrum (+ESI): 311 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691884B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-68d51c2c8e4446f191ef34c501b77790 |
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| Source note | uspto-grants-2010_04 |
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