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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740575Generated: October 31, 2026

1-(1-Benzylpiperidin-4-yl)-4-(4-fluorophenyl)-5-(4-pyridyl)imidazole → (1-Formyl piperidinyl)-4-(4-fluorophenyl)-5-(4-pyridinyl)imidazole

https://huagongshe.com/reaction/1740575

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Benzylpiperidin-4-yl)-4-(4-fluorophenyl)-5-(4-pyridyl)imidazoleHCID 11350454—
ReactantFormic acid methanolHCID 18963719—
CatalystPalladiumHCID 23938—
Product(1-Formyl piperidinyl)-4-(4-fluorophenyl)-5-(4-pyridinyl)imidazoleHCID 86754653—

Reaction Steps

1-(1-Benzylpiperidin-4-yl)-4(4-fluorophenyl)-5-(4-pyridyl)imidazole (100 mg; prepared in Example 40) was dissolved in 10% formic acid/methanol under argon and palladium black (100 mg) mixed in 10% formic acid/methanol was added. The reaction was stirred under argon at room temperature for sixteen hours. The reaction mixture was evaporated and the residue mixed in H2O/ethyl acetate and the pH taken to 10. The layers were separated and the aqueous phase extracted with ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969184
Source datasetuspto-grants-1999_10
ORD IDord-625e874e5525466ba58cb7d0fb4a567c
Source noteuspto-grants-1999_10