HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol hydrochloride → 1-{[(6S,7R)-7-(3,4-dichlorophenyl)-1,4-oxazepan-6-yl]methyl}-3-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)pyridin-2(1H)-one monohydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Reactant | tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-{[2-oxo-3-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)pyridin-1(2H)-yl]methyl}-1,4-oxazepane-4-carboxylate | HCID 136340695 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-{[(6S,7R)-7-(3,4-dichlorophenyl)-1,4-oxazepan-6-yl]methyl}-3-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)pyridin-2(1H)-one monohydrochloride | HCID 136340696 | 186.9% |
Reaction Steps
A 14 N hydrogen chloride-ethanol solution (2 mL, 28.00 mmol) was added to a solution of tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-{[2-oxo-3-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)pyridin-1(2H)-yl]methyl}-1,4-oxazepane-4-carboxylate (795 mg, 1.48 mmol) in ethanol (8 mL). The reaction mixture was stirred at room temperature for 3 hr, and at 80° C. for 15 min. The reaction mixture was concentrated under reduced pressure, and the residue was collected by filtration, and washed with ethanol-hexane to give the title compound (655 mg, 1.383 mmol, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722662B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-6ba9076f3c6c4117bcd6752f132e6ed3 |
| Source note | uspto-grants-2014_05 |