HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (S)-methyl 3-fluoro-4-(2-oxo-1-(piperidin-4-yl)pyrrolidin-3-yloxy)benzoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | (S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate | HCID 86688102 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-methyl 3-fluoro-4-(2-oxo-1-(piperidin-4-yl)pyrrolidin-3-yloxy)benzoate hydrochloride | HCID 67469793 | 100% |
Reaction Steps
To a solution of (S)-tert-butyl 4-(3-(2-fluoro-4-(methoxycarbonyl)phenoxy)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (2 g, 4.6 mmol) in EtOAc (20 mL) was added hydrogen chloride in isopropanol (5-6 M) (9.2 mL, 46 mmol) and the reaction was stirred overnight at ambient temperature. The reaction was concentrated under vacuum to give (S)-methyl 3-fluoro-4-(2-oxo-1-(piperidin-4-yl)pyrrolidin-3-yloxy)benzoate hydrochloride (1.5 g, 100%), which was used crude in the next reaction
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754226B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-beaa39158c704670aa5df9e55b611ec6 |
| Source note | uspto-grants-2014_06 |