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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251735Generated: October 25, 2026

Potassium Carbonate → N-[(cyclohexylamino)carbonyl]-3-[3-(4-phenoxy-2-propylphenoxy)propoxy]benzenesulfonamide

https://huagongshe.com/reaction/2251735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclohexyl isocyanateHCID 18502—
Reactant3-[3-(4-Phenoxy-2-propylphenoxy)propoxy]benzenesulfonamideHCID 58647129—
SolventAcetoneHCID 180—
ProductN-[(cyclohexylamino)carbonyl]-3-[3-(4-phenoxy-2-propylphenoxy)propoxy]benzenesulfonamideHCID 10053686—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 3-[3-(4-phenoxy-2-propyl phenoxy)propoxy]benzenesulfonamide (0.04 g, 0.0906 mmol) and acetone (3 mL) was added potassium carbonate (0.025 g, 0.181 mmol). To the resulting suspension was added cyclohexyl isocyanate (0.023 mL, 0.181 mmol) dropwise. The reaction suspension was then stirred in a 65° C. oil bath for 5 h. After cooling to room temperature, the reaction was concentrated to a residue. The residue was partitioned between ethyl acetate and water. The ethyl acetate phase was dried over sodium sulfate, filtered, and concentrated to an oil. The oil was chromatographed over silica gel with hexanes/ethyl acetate (4:1) and hexanes/ethyl acetate (3:1) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319170B2
Source datasetuspto-grants-2008_01
ORD IDord-0c9dae6624e04c3485932b706763af28
Source noteuspto-grants-2008_01