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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | 3-[3-(4-Phenoxy-2-propylphenoxy)propoxy]benzenesulfonamide | HCID 58647129 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[(cyclohexylamino)carbonyl]-3-[3-(4-phenoxy-2-propylphenoxy)propoxy]benzenesulfonamide | HCID 10053686 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07319170B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-0c9dae6624e04c3485932b706763af28 |
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| Source note | uspto-grants-2008_01 |
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