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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701971Generated: October 30, 2026

Hydrochloric Acid → HCID 20504611, compound

https://huagongshe.com/reaction/1701971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantHCID 20504601HCID 20504601—
CatalystMercuric oxideHCID 30856—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20504611HCID 20504611—

Reaction Steps

0.5 g N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamide)-ethyl]-benzenesulfonyl)-N'-cyclohexyl-isourea methyl ether (m.p. 138°-140° C., prepared by desulfurization of N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-cyclohexyl-thiourea with mercury oxide in the presence of methanol) is dissolved in 5 ml of dioxan, and heated for a short time on a steam bath with 2 ml of concentrated hydrochloric acid. Subsequently, the water is added to the reaction mixture, the product is suction-filtered, reprecipitated from dilute ammonia and recrystallized from dilute acetone. The N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-cyclohexyl urea obtained has a melting point of 176°-178° C. and, with the substance obtained according to Example 8, shows no depression.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379785
Source datasetuspto-grants-1983_04
ORD IDord-2ba0f4f39f9346e4934ff2ead7bc9df6
Source noteuspto-grants-1983_04