HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → n-(3-Acetylphenyl)-n'-((3s,4s)-4-{[4-(4-fluorobenzyl)cyclohexyl]amino}tetrahydro-3-furanyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(3-Isocyanatophenyl)ethan-1-one | HCID 312718 | — |
| Reactant | (3S,4S)-N3-[4-(4-fluorobenzyl)cyclohexyl]tetrahydro-3,4-furandiamine dihydrochloride | HCID 69587943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-(3-Acetylphenyl)-n'-((3s,4s)-4-{[4-(4-fluorobenzyl)cyclohexyl]amino}tetrahydro-3-furanyl)urea | HCID 9911755 | 66.1% |
Reaction Steps
To a stirring solution of (3S,4S)-N3-[4-(4-fluorobenzyl)cyclohexyl]tetrahydro-3,4-furandiamine dihydrochloride (20 mg, 0.055 mmol) and triethylamine (100 μL, 0.72 mmol) in dichloromethane (1 mL) was added 3-acetylphenyl isocyanate (7.1 mg, 0.050 mmol). The resulting solution was immediately concentrated, and the resulting residue was purified by flash column chromatography (100% ethyl acetate then 5% triethylamine in ethyl acetate then 10% methanol in ethylacetate containing 5% triethylamine) to yield the desired urea (15 mg, 60%) as an oily white solid. MS (ESI) 454 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608227B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-79ed37a1ec004b98a90c5fb1c55d44a1 |
| Source note | uspto-grants-2003_08 |