HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(4,5,6,7-Tetrafluoro-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-2,6-piperidinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminopiperidine-2,6-dione hydrochloride | HCID 134548 | — |
| Reactant | HCID 21928258 | HCID 21928258 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4,5,6,7-Tetrafluoro-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-2,6-piperidinedione | HCID 12972138 | — |
Reaction Steps
A mixture of 16.25 g of 2,6-dioxopiperidin-3-ammonium chloride, and 30.1 g of methyl 2-bromomethyl-3,4,5,6-tetrafluorobenzoate, and 12.5 g of triethylamine in 100 mL of dimethylformamide is stirred at room temperature for 15 hours. The mixture is then concentrated in vacuo and the residue mixed with methylene chloride and water. The aqueous layer is separated and back-extracted with methylene chloride. The combined methylene chloride solutions are dried over magnesium sulfate and concentrated in vacuo to give 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4,5,6,7-tetrafluoroisoindoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05798368 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-f41402320525423dbc3ed45f39912e3a |
| Source note | uspto-grants-1998_08 |