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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424613Generated: October 28, 2026

2,5-Dimethylpiperazine → HCID 67010994, compound

https://huagongshe.com/reaction/2424613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DimethylpiperazineHCID 7816—
ReactantTriethylamineHCID 8471—
Reactant2-(Trifluoromethyl)benzoyl chlorideHCID 67561—
Reactant6-Chloropyridazine-3-carboxylic acid pentylamideHCID 44203153—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
ProductHCID 67010994HCID 6701099462.8%

Reaction Steps

To a mixture of 6-chloropyridazine-3-carboxylic acid pentylamide (304 mg, 1.00 mmol) in 2-propanol (12 mL) was added 2,5-dimethylpiperazine (1.37 g, 12.0 mmol). The reaction mixture was refluxed for 2 days. Another 0.25 g of 2,5-dimethylpiperazine and 1.0 mL of triethylamine were added to the reaction mixture and heating was continued for another 24 hours. After the reaction mixture was cooled to ambient temperature and the solvent was removed by rotary evaporator. To the dichloromethane solution of the crude material (20 mL) was added the solution of 2-trifluoromethylbenzoyl chloride (0.63 g, 3.00 mmol) in dichloromethane (20 mL) and the reaction mixture was stirred at ambient temperature for 16 hours. The organic layer was diluted with dichloromethane (50 mL) and then washed with 10% HCl, dried over MgSO4. After filtration, the filtrate was concentrated in vacuo. The crude material was purified by column chromatography eluting with ethyl acetate (100%) to afford 300 mg (31% yield) of the product as a colourless solid. 1H NMR (300 MHz, CDCl3) δ 7.74-7.43, 7.36-7.24, 5.17-5.04, 4.91-4.79, 4.52, 4.52, 3.68-3.57, 3.54-3.44, 3.39-3.11, 2.93, 2.85-2.71, 1.36-1.31, 1.27-1.15, 1.23-1.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964591B2
Source datasetuspto-grants-2011_06
ORD IDord-5a12da21953543b0a23f4cec9840b91d
Source noteuspto-grants-2011_06