Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359983Generated: October 30, 2026

Fenbufen → HCID 86623036, compound

https://huagongshe.com/reaction/1359983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFenbufenHCID 3335—
ReactantDichloromethaneHCID 6344—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactantt-Butoxycarbonyl-aminopropanolHCID 23149331—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
ProductHCID 86623036HCID 8662303683%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879817B2
Source datasetuspto-grants-2011_02
ORD IDord-7a677bca2c8147919bab7a69f44ba6b6
Source noteuspto-grants-2011_02