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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664781Generated: November 1, 2026

Benzyl 4-(6-methyl-3-oxo-2,3,4,5-tetrahydropyridazine-4-yl)piperidine-1-carboxylate → HCID 67438530, compound

https://huagongshe.com/reaction/1664781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(6-methyl-3-oxo-2,3,4,5-tetrahydropyridazine-4-yl)piperidine-1-carboxylateHCID 67438628—
CatalystCupric ChlorideHCID 24014—
SolventAcetonitrileHCID 6342—
ProductHCID 67438530HCID 6743853058.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

Copper(II) chloride (anhydrous; 2.02 g, 15.05 mmol) was added to a solution of benzyl 4-(6-methyl-3-oxo-2,3,4,5-tetrahydropyridazine-4-yl)piperidine-1-carboxylate (2.48 g, 7.53 mmol) in acetonitrile (26 mL). The reaction mixture was heated at 90° C. After 18 h, the mixture was cooled to ambient temperature and concentrated. The residue was diluted with dichloromethane and 1 N HCl. The mixture was extracted with dichloromethane (3×), and the combined organic extracts were dried over magnesium sulfate and concentrated. Purification by silica gel chromatography (100% dichloromethane→90% dichloromethane/methanol) to give the title compound (1.45 g). MS 328.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-75946abccaf34d2cb171d2e2e597d7ce
Source noteuspto-grants-2011_10