HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol hydrochloride → (1S)-1-[(6R,7R)-6-(3,4-dichlorophenyl)-1,4-oxazepan-7-yl]ethane-1,2-diol monohydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Reactant | tert-butyl (6R,7R)-6-(3,4-dichlorophenyl)-7-[(1S)-1,2-dihydroxyethyl]-1,4-oxazepane-4-carboxylate | HCID 66975748 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1S)-1-[(6R,7R)-6-(3,4-dichlorophenyl)-1,4-oxazepan-7-yl]ethane-1,2-diol monohydrochloride | HCID 66975464 | 179.2% |
Reaction Steps
To a solution of tert-butyl (6R,7R)-6-(3,4-dichlorophenyl)-7-[(1S)-1,2-dihydroxyethyl]-1,4-oxazepane-4-carboxylate (450 mg) in ethanol (8 mL) was added 12 mol/kg hydrogen chloride-ethanol solution (8 mL), and the mixture was stirred at room temperature for 15 min. The solvent was evaporated under reduced pressure, and the residue was crystallized from water-ethanol-diethyl ether to give the title compound (340 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722662B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-9f19eb70ae8b45758c442362e9660159 |
| Source note | uspto-grants-2014_05 |