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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398274Generated: October 30, 2026

Hydrochloric Acid → HCID 22500834, compound

https://huagongshe.com/reaction/398274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 22500714HCID 22500714—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductHCID 22500834HCID 2250083490.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

4N HCl (5mL) 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610734B2
Source datasetuspto-grants-2003_08
ORD IDord-86f0c3ef01554d3382b304d3b1f2380f
Source noteuspto-grants-2003_08