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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043082Generated: November 1, 2026

Hydrochloric Acid → 5-Chloro-2-methoxy-N-(2-(1-(3-cyclopropylureidosulfonyl)piperidin-4-yl)ethyl)benzamide

https://huagongshe.com/reaction/2043082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
Reactant5-Chloro-2-methoxy-N-(2-(1-(3-cyclopropylthioureidosulfonyl)piperidin-4-yl)ethyl)benzamideHCID 59660709—
SolventSodium HydroxideHCID 14798—
Product5-Chloro-2-methoxy-N-(2-(1-(3-cyclopropylureidosulfonyl)piperidin-4-yl)ethyl)benzamideHCID 5966071032.7%

Reaction Steps

0.2 ml (2.32 mmol) of 30% strength hydrogen peroxide solution was added to a solution of 96 mg (0.2 mmol) of 5-chloro-2-methoxy-N-(2-(1-(3-cyclopropylthioureidosulfonyl)piperidin-4-yl)ethyl)benzamide in 2 ml of 0.5 M sodium hydroxide solution at 0° C. After the reaction mixture had been kept at 0° C. for 1 hour, 200 mg of sodium sulfite were added, and the mixture was acidified by means of 2 M hydrochloric acid. The precipitated solid was filtered off, washed with water until neutral and purified by chromatography (silica gel; toluene/ethanol/ethyl acetate 8/1/1). The crude product was crystallized from methanol. 30 mg (32%) of the title compound were obtained as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586612B2
Source datasetuspto-grants-2013_11
ORD IDord-122c1c287d164ce9abdab0e8b639181a
Source noteuspto-grants-2013_11