HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251732Generated: October 26, 2026
Potassium Carbonate → N-[(cyclohexylamino)carbonyl]-4-[3-(4-phenoxy-2-propylphenoxy)propoxy]benzenesulfonamide
https://huagongshe.com/reaction/2251732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Cyclohexyl isocyanate | HCID 18502 | — |
| Reactant | 4-[3-(4-Phenoxy-2-propylphenoxy)propoxy]benzenesulfonamide | HCID 58647128 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[(cyclohexylamino)carbonyl]-4-[3-(4-phenoxy-2-propylphenoxy)propoxy]benzenesulfonamide | HCID 9850927 | — |
Reaction Steps
To a solution of 4-[3-(4-phenoxy-2-propyl phenoxy)propoxy]benzenesulfonamide (0.045 g, 0.102 mmol) and acetone (3 mL) was added potassium carbonate (0.028 g, 0.204 mmol). To the resulting suspension was added cyclohexyl isocyanate (0.026 mL, 0.204 mmol) dropwise. The reaction suspension was then stirred in a 65° C. oil bath for 6 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 obtain 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-8cadbd035cb24d7dbb22b5b977f2f8b2 |
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| Source note | uspto-grants-2008_01 |
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