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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258159Generated: November 1, 2026

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

https://huagongshe.com/reaction/1258159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[(3,5-Difluorophenyl)methyl]piperidin-4-amineHCID 22182400—
Reactant6-Chloro-4,5-dimethyl-pyridazine-3-carbonitrileHCID 59253659—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-[1-(3,5-Difluoro-benzyl)-piperidin-4-ylamino]-4,5-dimethyl-pyridazine-3-carbonitrileHCID 5925365642%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 6-chloro-4,5-dimethyl-pyridazine-3-carbonitrile (D11) (0.120 g, 0.72 mmol), 1-(3,5-difluoro-benzyl)-piperidin-4-ylamine (D5) (0.194 g, 0.86 mmol) and diisopropylethylamine (0.188 ml, 1.08 mmol) in acetonitrile was stirred at 180° C. for 20 min., under microwave irradiation (Biotage MW-oven), and then again at 180° C. for additional 30 min. Dichloromethane, water and a saturated solution of sodium carbonate were then added. The organic phase was separated, filtered over cotton and evaporated in vacuo. The residue was purified by column chromatography (silica gel; 0-1% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and the solvent evaporated in vacuo to yield E19 (0.108 g, 42%) as a solid. C19H21F2N5 requires 357. Found 358 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466153B2
Source datasetuspto-grants-2013_06
ORD IDord-d9fe36792021470db79704d6120dada9
Source noteuspto-grants-2013_06