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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258155Generated: October 31, 2026

Sodium Carbonate → 6-[1-(3,5-Difluoro-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile

https://huagongshe.com/reaction/1258155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloropyridazine-3-carbonitrileHCID 13382871—
Reactant1-[(3,5-Difluorophenyl)methyl]piperidin-4-amineHCID 22182400—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-[1-(3,5-Difluoro-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrileHCID 2498919960.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 6-chloro-pyridazine-3-carbonitrile (D4) (1.74 g, 12.46 mmol), 1-(3,5-difluoro-benzyl)-piperidin-4-ylamine (D5) (2.35 g, 10.386 mmol) and diisopropylethylamine (2.71 ml, 15.58 mmol) in acetonitrile (30 ml) was stirred at 120° C. for 40 min., under microwave irradiation (Milestone MW-oven). Dichloromethane, water and a saturated solution of sodium carbonate were then added. The organic layers were filtered over cotton, evaporated in vacuo and the residue was purified by column chromatography (silica gel; 0-1.5% ammonia in methanol (7 M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The residue was precipitated in heptane to yield E15 (2.065 g, 60%) as a solid. C17H17F2N5 requires 329. Found 330 (MH+); mp: 187.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-d2137ceb23bf4496bde63be1f388efed
Source noteuspto-grants-2013_06