Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453647Generated: October 26, 2026

Diisopropylethylamine → 2-{4-[4-(2-tert-Butyl-6-trifluoromethyl-pyrimidin-4-yl)-piperazin-1-yl]butyl}-2H-[1,2,4]triazine-3,5-dione hydrochloride

https://huagongshe.com/reaction/453647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BromideHCID 253881—
Reactant2-(4-Chloro-butyl)-2H-[1,2,4]triazine-3,5-dioneHCID 15817175—
Reactant2-(tert-Butyl)-4-(piperazin-1-yl)-6-(trifluoromethyl)pyrimidineHCID 18399610—
SolventDimethylformamideHCID 6228—
Product2-{4-[4-(2-tert-Butyl-6-trifluoromethyl-pyrimidin-4-yl)-piperazin-1-yl]butyl}-2H-[1,2,4]triazine-3,5-dione hydrochlorideHCID 67512270—

Reaction Steps

13.4 g of 2-(4-chloro-butyl)-2H-[1,2,4]triazine-3,5-dione (65.8 mmol) and 18.97 g of 2-tert-butyl-4-piperazin-1-yl-6-trifluoromethyl-pyrimidine (65.8 mmol) were dissolved in 400 mL of dimethylformamide. After addition of 33.9 g of sodium bromide (329 mmol) and 115 mL of N,N-diisopropylethylamine (658 mmol), the reaction was stirred for 48 h at room temperature. Then the solvent was removed under reduced pressure and the obtained residue was trituated with 400 mL of ethyl acetate and the obtained solution was filtered. The filtrate was evaporated to dryness and the remaining oily residue was treated with 100 mL of diethyl ether, filtered and the filtrate was again evaporated to dryness. The crude product was purified three times via silica gel chromatography (ethyl acetate-methanol 0-100%; dichloromethane-methanol 0-5%; dichloro-methane-methanol 0-2%) to yield the free base of the title compound. This product was transferred into its hydrochloride salt via treatment with HCl/diethyl ether (yield 2.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492540B2
Source datasetuspto-grants-2013_07
ORD IDord-653ba22409ef4710a04fb53f33b90b3e
Source noteuspto-grants-2013_07