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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459785Generated: October 30, 2026

Triethylamine → HCID 58824141, compound

https://huagongshe.com/reaction/459785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 58824132HCID 58824132—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58824141HCID 58824141789.1%

Reaction Steps

To a solution of 4-(3-Amino-2-cyano-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (0.976 g, 3.23 mmol) and NEt3 (0.9 ml, 6.48 mmol) in THF (40 ml) was added 4-fluoro-benzoyl chloride (0.42 ml, 0.355 mmol). The solution was stirred with a magnetic stirrer at room temperature overnight and the reaction mixture was partitioned between water and ethyl acetate. The organic layer was washed with water (2×30 ml) and brine (30 ml). After drying over MgSO4, the organic fraction was concentrated in vacuo and resulting brown residue was purified by flash chromatography to give 4-[2-cyano-3-(4-fluoro-benzoylamino)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester as a yellow solid (1.189 g, 87%). MS: (M+H)+425.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196087B2
Source datasetuspto-grants-2007_03
ORD IDord-2df7f484b3244605bd0c56d0dacb69b8
Source noteuspto-grants-2007_03