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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827589Generated: November 1, 2026

Hydrochloric Acid → HCID 22137342, compound

https://huagongshe.com/reaction/1827589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 22137380HCID 22137380—
SolventEthanolHCID 702—
ProductHCID 22137342HCID 22137342—

Reaction Steps

The crude N-(4-methoxy-phenyl)-2,4,6-trimethyl-N-[4-(tetrahydro-pyran-2-yloxy)-benzyl]-benzenesulfonamide prepared in Step A was suspended in 2 mL of a 3:1 (v/v) mixture of ethanol:1N HCl and was stirred at room temperature overnight. The reaction mixture was quenched with saturated aqueous sodium bicarbonate and the aqueous solution was washed with methylene chloride. The organic layer was concentrated. The residue was purified by reverse phase HPLC (98:2 water:0.1% trifluoracetic acid to 98:2 acetonitrile:water) to afford the title compound. MS 411 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053212B2
Source datasetuspto-grants-2006_05
ORD IDord-86864bdd6fd8407bb7f465af17d30c4f
Source noteuspto-grants-2006_05