HuagongsheHuagongshe Chemistry Print Report · For research reference only
Flurbiprofen → HCID 86623032, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Flurbiprofen | HCID 3394 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | t-Butoxycarbonyl-aminopropanol | HCID 23149331 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86623032 | HCID 86623032 | 94% |
Reaction Steps
In 2 ml of dichloromethane, 352 mg (2 mmol) of Boc-aminopropanol and 489 g (2 mmol) of flurbiprofen (manufactured by Wako Pure Chemical Industries) were dissolved, and 48 mg (0.4 mmol) of DMAP and 423 g (2.2 mmol) of WSCI.HCl/2 ml dichloromethane were added thereto in this order under ice-cooling. After returning to room temperature and stirring overnight, ethyl acetate was added thereto, followed by separation by washing with 5% citric acid twice, water, 5% sodium hydrogen carbonate twice, water and saturated brine consecutively. After dehydration drying with sodium sulfate, ethyl acetate was evaporated under reduced pressure to give 753 mg of the titled compound (yield 94%). The structure was identified by 1H-NMR (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879817B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-086dc3146ad04293bcb3002b5d955634 |
| Source note | uspto-grants-2011_02 |