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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056898Generated: October 30, 2026

3-Aminobiphenyl → 5-(benzyloxy)-1-biphenyl-3-yl-2-methylpyridin-4(1H)-one

https://huagongshe.com/reaction/1056898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminobiphenylHCID 16717—
Reactant5-(Benzyloxy)-2-methyl-4H-pyran-4-oneHCID 5314171—
SolventAcetic AcidHCID 176—
Product5-(benzyloxy)-1-biphenyl-3-yl-2-methylpyridin-4(1H)-oneHCID 67419356—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a suspension of 6.6 g (30.5 mmol) 5-(benzyloxy)-2-methyl-4H-pyran-4-one in 150 ml 30% AcOH was added 7.5 g (45.8 mmol) m-aminobiphenyl. The reaction mixture was heated at 160° C. for 18 h, then cooled to rt, extracted with 300 ml EtOAc, washed with brine, and concentrated in vacuo. Purification by flash chromatography (330 g silica gel, 0-20% MeOH:EtOAc) afforded 5-(benzyloxy)-1-biphenyl-3-yl-2-methylpyridin-4(1H)-one. LCMS (M+H)+=368.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399651B2
Source datasetuspto-grants-2016_07
ORD IDord-20693faa630b4039bf98a16416dd299e
Source noteuspto-grants-2016_07