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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258158Generated: November 1, 2026

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

https://huagongshe.com/reaction/1258158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Chloropyridazine-3-carbonitrileHCID 13382871—
Reactant1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamineHCID 53256189—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-[1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrileHCID 2498920174%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 6-chloro-pyridazine-3-carbonitrile (D4) (1.32 g, 9.46 mmol), 1-(3,4,5-trifluoro-benzyl)-piperidin-4-ylamine (D8) (2.10 g, 8.6 mmol) and diisopropylethylamine (2.25 ml, 12.9 mmol) in acetonitrile (12 ml) was stirred at 120° C. for 20 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; 0-2% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The residue was precipitated from diisopropyl ether to yield E18 (2.210 g, 74%) as a solid. C17H16F3N5 requires 347. Found 348 (MH+); mp: 185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-b37c9399d4f249f2a91a78c9019f2b47
Source noteuspto-grants-2013_06