HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen chloride-ethyl acetate → 9-(3,3-Difluoropyrrolidin-1-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | HCID 68578493 | HCID 68578493 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 9-(3,3-Difluoropyrrolidin-1-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine | HCID 68578558 | 52% |
Reaction Steps
A mixture of tert-butyl 9-(3,3-difluoropyrrolidin-1-yl)-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (110 mg, 0.310 mmol), ethyl acetate (2 ml) and 4N hydrogen chloride-ethyl acetate solution (2 ml) was stirred at room temperature for 1 hr, and the solvent was evaporated under reduced pressure. The residue was added to 1N aqueous sodium hydroxide solution (2 ml), and the mixture was extracted with ethyl acetate:tetrahydrofuran (1:1). The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by NH silica gel column chromatography (hexane:ethyl acetate=1:1) to give the desired product (41.0 mg, 52.0%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247403B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-397d2cd3ff9e47fcbf701ac8ff11ea63 |
| Source note | uspto-grants-2012_08 |