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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854812Generated: November 1, 2026

Triethylamine → HCID 53493384, compound

https://huagongshe.com/reaction/1854812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
Reactant3-(Piperazin-1-yl)-1,2,4-triazineHCID 12296696—
SolventDichloromethaneHCID 6344—
ProductHCID 53493384HCID 5349338495%

Reaction Steps

Compound 3 is prepared according to synthesis method 2: 0.4 g (2.42 mmoles) of derivative 5a is placed in 10 ml of CH2Cl2. 0.5 ml (3.63 mmoles) of triethylamine is added. At 0° C., 0.4 ml (2.66 mmoles) of trifluoromethylbenzoyl chloride is added drop by drop, the reaction medium is stirred at ambient temperature for 18 hours. After concentrating the reaction medium to dryness, the residue obtained is taken up with AcOEt and washed with water. After drying on MgSO4, the organic phase is concentrated. The residue obtained is purified by silica flash chromatography (CH2Cl2,100%). 0.72 g of yellow powder is isolated (yield: 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962837B2
Source datasetuspto-grants-2015_02
ORD IDord-442549949af141279dab38c84a19b011
Source noteuspto-grants-2015_02