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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225433Generated: October 30, 2026

Sulfamide → HCID 19004203, compound

https://huagongshe.com/reaction/2225433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamideHCID 82267—
ReactantHCID 19004206HCID 19004206—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 19004203HCID 1900420341.7%

Reaction Steps

A solution of 1-(4-aminophenethyl)-4-(diphenylmethoxymethyl)piperidine (200 mg, 0.50 mmol) (see Example 21) and sulphamide (480 mg, 5.0 mmol) in dioxane (5 ml) was heated under reflux for 3 hours and evaporated. The residue was partitioned between ethyl acetate and 10% aqueous potassium carbonate solution and the layers separated. The aqueous layer was extracted into ethyl acetate and the combined organic layers were dried over magnesium sulphate and evaporated. The residue was purified by chromatography on silica using dichloromethane plus 0-4% methanol as eluant. Appropriate fractions were combined and evaporated and the residue triturated with diisopropyl ether. The resulting solid was collected, washed with diisopropyl ether and dried to give the title compound (100 mg) as a pale yellow solid, m.p. 172°-174° C., which was characterised by its 1H-NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344835
Source datasetuspto-grants-1994_09
ORD IDord-0fe991cb61d14827a1ea0e663580f094
Source noteuspto-grants-1994_09