Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Fenbufen | HCID 3335 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| 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 | Ethyl Acetate | HCID 8857 | — |
| Solvent | dichloromethane N,N-dimethylformamide | HCID 22350042 | — |
| Product | HCID 86623036 | HCID 86623036 | 83% |
Reaction Steps
Boc-aminopropanol (2.18 mmol), fenbufen (2.18 mmol) (manufactured by ICN Biochemicals Inc.) and DMAP (0.44 mmol) were dissolved in DMF-dichloromethane (5:3, 8 ml), and dichloromethane solution (5 ml) of WSCI.HCl (2.48 mmol) was added thereto under ice-cooling. After gradually returning the reaction temperature to room temperature, the mixture was stirred overnight. Ethyl acetate was added thereto, followed by separation by washing with 5% aqueous citric acid solution, 5% aqueous sodium hydrogen carbonate solution and saturated brine consecutively. After dehydration drying with sodium sulfate, the solvent was evaporated under reduced pressure. The thus obtained residue was purified by silica gel column chromatography (chloroform:ethyl acetate=40:1, 0.5% triethylamine) to give the titled compound (747.8 mg, yield 83%). The structure was identified by 1H-NMR (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879817B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-7a677bca2c8147919bab7a69f44ba6b6 |
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| Source note | uspto-grants-2011_02 |
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