HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (S)-benzyl 2-oxo-1,4'-bipiperidin-3-ylcarbamate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | (S)-tert-butyl 3-(benzyloxycarbonylamino)-2-oxo-1,4'-bipiperidine-1'-carboxylate | HCID 58787267 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-benzyl 2-oxo-1,4'-bipiperidin-3-ylcarbamate hydrochloride | HCID 86688092 | 100% |
Reaction Steps
A flask was charged with (S)-tert-butyl 3-(benzyloxycarbonylamino)-2-oxo-1,4′-bipiperidine-1′-carboxylate (Example 39, Steps A-B; 10.0 g, 23.2 mmol), DCM (60 mL), methanol (6 mL), HCl (57.9 mL, 232 mmol) and the reaction was stirred overnight. The organic solvents were removed under reduced pressure to provide (S)-benzyl 2-oxo-[1,4′-bipiperidin]-3-ylcarbamate hydrochloride (8.52 g, 100% yield). Mass spectrum (apci) m/z=332.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754226B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-6b613b7cffc34186a07bf6914ed5072f |
| Source note | uspto-grants-2014_06 |