HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5-(3,4-Difluorophenyl)-2,3-dihydro-4-methoxycarbonyl-1-(3-(4-methoxycarbonyl-4-phenylpiperidin-1-yl)prop-1-yl) aminocarbonyl-2(1H)-imidazolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Aminopropyl)-4-methoxycarbonyl-4-phenylpiperidine | HCID 10683883 | — |
| Reactant | 1-trichloroacetyl-5-(3,4-difluorophenyl)-2,3-dihydro-4-methoxycarbonyl-2(1H)-imidazolone | HCID 18798271 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(3,4-Difluorophenyl)-2,3-dihydro-4-methoxycarbonyl-1-(3-(4-methoxycarbonyl-4-phenylpiperidin-1-yl)prop-1-yl) aminocarbonyl-2(1H)-imidazolone | HCID 18798277 | 2% |
Reaction Steps
A mixture of 1-trichloroacetyl-5-(3,4-difluorophenyl)-2,3-dihydro-4-methoxycarbonyl-2(1H)-imidazolone (583 mg, 1.46 mmol), 1-(3-aminopropyl)-4-methoxycarbonyl-4-phenylpiperidine (808 mg, 2.92 mmol) and potassium carbonate (809 mg, 5.85 mmol) in dioxane (15 mL) was heated at reflux for 24 hours and then concentrated. The residue was partitioned between EtOAc and water. The organic layer was dried over Na2SO4, filtered and concentrated to give the crude product which was flash chromatographed over silica gel to give the product (15 mg, 2% yield). Hydrochloride salt: light brown solid; m.p. 134-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046331 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-9d49694ebe004365942cb81ef6ea5782 |
| Source note | uspto-grants-2000_04 |