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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664780Generated: November 1, 2026

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

https://huagongshe.com/reaction/1664780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantBenzyl 4-[1-(ethoxycarbonyl)-3-oxobutyl]piperidine-1-carboxylateHCID 67438602—
SolventAcetic AcidHCID 176—
ProductBenzyl 4-(6-methyl-3-oxo-2,3,4,5-tetrahydropyridazine-4-yl)piperidine-1-carboxylateHCID 67438628—

Reaction Conditions

Temperature50 °C

Reaction Steps

Hydrazine (4.72 mL, 148.7 mmol) was added to a solution of benzyl 4-[1-(ethoxycarbonyl)-3-oxobutyl]piperidine-1-carboxylate (2.69 g, 7.44 mmol) in acetic acid (110 mL). The reaction mixture was heated at 50° C. After 1 h, the reaction mixture was concentrated. The residue was diluted with dichloromethane, neutralized by saturated aqueous sodium bicarbonate. The mixture was extracted with dichloromethane (3×), and the combined organic extracts were dried over magnesium sulfate and concentrated to give the title compound. MS 330.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-c29e158e98c84ad5aa6f438638272007
Source noteuspto-grants-2011_10