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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360003Generated: October 30, 2026

Diclofenac → HCID 178458017, compound

https://huagongshe.com/reaction/1360003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiclofenacHCID 3033—
ReactantEthyl AcetateHCID 8857—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 71650669HCID 71650669—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 178458017HCID 178458017157,164.297%

Reaction Steps

In 3 ml of dichloromethane, 338.4 mg (1.94 mmol) of tert-butyl N-(2-aminopropyl)carbamic acid (manufactured by Tokyo Kasei Kogyo) and 694.4 mg (2.34 mmol) of diclofenac were dissolved, and under ice-cooling, 59.0 mg (0.483 mmol) of DMAP and 505.3 mg (2.64 mmol) of WSCI.HCl were added thereto, followed by stirring for 70 minutes and then stirred at room temperature for 90 minutes. 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 with sodium sulfate, ethyl acetate was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to give 835.5 g (95%) of the titled compound. The structure was identified by 1H-NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879817B2
Source datasetuspto-grants-2011_02
ORD IDord-b8b0bbfc68c74bfb9213ac7e22e6ed50
Source noteuspto-grants-2011_02