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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258156Generated: November 2, 2026

Dichloromethane → 6-[1-(3-Trifluoromethyl-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile

https://huagongshe.com/reaction/1258156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-{[3-(Trifluoromethyl)phenyl]methyl}piperidin-4-amineHCID 12888929—
Reactant6-Chloropyridazine-3-carbonitrileHCID 13382871—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product6-[1-(3-Trifluoromethyl-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrileHCID 2498920064%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 6-chloro-pyridazine-3-carbonitrile (D4) (0.130 g, 0.931 mmol), 1-(3-trifluoromethyl-benzyl)-piperidin-4-ylamine (D6) (0.241 g, 0.931 mmol) and diisopropylethylamine (0.243 ml, 1.4 mmol) in acetonitrile (3 ml) was stirred at 120° C. for 30 min., under microwave irradiation (Biotage MW-oven). Dichloromethane and water were added, and then the mixture washed with a saturated solution of sodium carbonate. The organic phase was filtered over cotton and the solvent was evaporated in vacuo. The residue was purified by column chromatography (silica gel; 0-2% ammonia in methanol (7M)/dichloromethane) to yield E16 (0.215 g, 64%) as a solid. C18H18F3N5 requires 361. Found 362 (MH+); mp: 170.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-f1c8b74b93d24522ab353a550e988c22
Source noteuspto-grants-2013_06