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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325155Generated: October 27, 2026

Hydrochloric Acid → [6-(n-Hexylsulfonoyl)-2-[4-(n-hexylsulfonoyl)phenyl]benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]-phenyl] methanone, Hydrochloride

https://huagongshe.com/reaction/325155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant[6-(n-Hexylsulfonoyl)-2-[4-(n-hexylsulfonoyl)phenyl]benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]-phenyl] methanoneHCID 18357255—
SolventEthyl AcetateHCID 8857—
Product[6-(n-Hexylsulfonoyl)-2-[4-(n-hexylsulfonoyl)phenyl]benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]-phenyl] methanone, HydrochlorideHCID 131722013—

Reaction Steps

[6-(n-Hexylsulfonoyl)-2-[4-(n-hexylsulfonoyl)phenyl]benzo[b]thien-3-yl][4-[2-(1-piperidinyl)ethoxy]-phenyl] methanone (3 g) was dissolved in 20 ml of ethyl acetate and hydrochloric acid-saturated diethyl ether was added. No precipitate formed. The reaction mixture was evaporated to a thick oil and was triturated several times with diethyl ether and dried in vacuo at room temperature to afford 1.64 g of the title compound as a white amorphous and hygroscopic powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221838B1
Source datasetuspto-grants-2001_04
ORD IDord-ce98a606eb8543fdae1311e4f34ea62d
Source noteuspto-grants-2001_04