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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664793Generated: November 2, 2026

HCID 67439310, compound → Benzyl 4-(6-cyclopropyl-3-oxo-2,3-dihydropyridazin-4-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1664793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67439310HCID 67439310—
CatalystCupric ChlorideHCID 24014—
SolventAcetonitrileHCID 6342—
ProductBenzyl 4-(6-cyclopropyl-3-oxo-2,3-dihydropyridazin-4-yl)piperidine-1-carboxylateHCID 6743992040.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

Copper(II) chloride (anhydrous; 101 mg, 0.75 mmol) was added to a solution of benzyl 4-(6-cyclopropyl-3-oxo-2,3,4,5-tetrahydropyridazine-4-yl)piperidine-1-carboxylate (134 mg, 0.38 mmol) in acetonitrile (16 mL). The reaction mixture was heated to 90° C. After 18 h, the mixture was cooled to ambient temperature and concentrated. Dichloromethane was added to the concentrated mixture, followed by hydrochloric acid (1 N in water). 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) gave the title compound (54 mg). MS 354.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-ca7ce683feea4450afe5244e858ed9d3
Source noteuspto-grants-2011_10