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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172756Generated: November 2, 2026

Triethylamine → HCID 11211291, compound

https://huagongshe.com/reaction/1172756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 66618243HCID 66618243—
SolventDichloromethaneHCID 6344—
ProductHCID 11211291HCID 1121129136.3%

Reaction Steps

To a suspension of 2-[3-(4-fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-1-methyl-piperazine dihydrochloride (0.285 g, 0.86 mmol) in anhydrous dichloromethane (6 mL), under nitrogen atmosphere, triethylamine (374 mL, 2.7 mmol) and 4-fluorobenzoyl chloride (102 mL, 0.86 mmol) were subsequently added at 0° C. The reaction mixture was allowed to warm at room temperature and stirred for 2 h. NaOH 1N (6 mL) was added and the phases were separated. The organic layer was washed sequentially with NaOH 1N (6 mL) and with water, then was dried over sodium sulphate and evaporated under reduced pressure. Purification of the crude by flash chromatography (silica gel, eluent: DCM/MeOH/NH4OH 99/1/0.1) afforded (4-fluoro-phenyl)-{3-[3-(4-fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-4-methyl-piperazine-1-yl}-methanone (0.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834035B2
Source datasetuspto-grants-2010_11
ORD IDord-b17fe56bd8dd4109b2294b77a3c379fc
Source noteuspto-grants-2010_11