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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713148Generated: November 1, 2026

Sodium Iodide → 7-[2-(4-Cyclobutylpiperazin-1-yl)-2-oxoethyl]-3-chloro-5,6,7,8-tetrahydropyrido[3,4-c]pyridazine

https://huagongshe.com/reaction/1713148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-(4-cyclobutyl-piperazine) acetamideHCID 66877902—
Reactant3-chloro-5H,6H,7H,8H-pyrido(3,4-c)pyridazine hydrochlorideHCID 86346446—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7-[2-(4-Cyclobutylpiperazin-1-yl)-2-oxoethyl]-3-chloro-5,6,7,8-tetrahydropyrido[3,4-c]pyridazineHCID 59463564—

Reaction Steps

To a stirred solution of 3-chloro-5,6,7,8-tetrahydropyrido[3,4-c]pyridazine hydrogen chloride salt (0.9 g) in acetonitrile (10.0 ml) is added 2-chloro-(4-cyclobutyl-piperazine)-acetamide (1 g), K2CO3 (1.6 g), and NaI (50 mg). The resulting mixture is stirred at rt overnight. Water (20.0 ml) is added to quench the reaction, and then the acetonitrile is evaporated. The residue is extracted with DCM (20 ml×3). The combined organic phase is dried over sodium sulfate, and the solvent is removed under reduced pressure to give a residue which is purified by silica gel chromatography (EtOAc/4% TEA) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795262B2
Source datasetuspto-grants-2010_09
ORD IDord-52de19e2aa23424ea75abb87c23142da
Source noteuspto-grants-2010_09