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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423194Generated: October 26, 2026

Triethylamine → HCID 178485438, compound

https://huagongshe.com/reaction/423194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(Dimethylamino)pyridiniumHCID 2735020—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 178524388HCID 178524388—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178485438HCID 17848543864%

Reaction Steps

To a mixture of 5-cyclohexyl-3-hydroxy-1-(4-isoxazol-3-ylphenyl)-4-(4-carboxybenzoyl)-1,5-dihydropyrrol-2-one (0.095 g, 0.2 mmol) and DMF (2 mL) was added, methylamine hydrochloride (0.020 g, 0.3 mmol), 1-hydroxybenztriazole (0.041 g, 0.3 mmol), 4-dimethylaminopyridinium (0.005 g, 0.04 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.058 g, 0.3 mmol) and triethylamine (0.042 mL, 0.3 mmol). The mixture was stirred at r.t. for 1 hr. Ethyl acetate and water were added, and the precipitate was collected by filtration to give 5-cyclohexyl-3-hydroxy-1-(4-isoxazol-3-ylphenyl)-4-(4-methylcarbamoylbenzoyl)-1,5-dihydropyrrol-2-one (0.062 g, 64%) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101644B2
Source datasetuspto-grants-2012_01
ORD IDord-429bc179e9554cdcacdf0fbf191e0880
Source noteuspto-grants-2012_01