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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Aminobiphenyl | HCID 16717 | — |
| Reactant | 5-(Benzyloxy)-2-methyl-4H-pyran-4-one | HCID 5314171 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(benzyloxy)-1-biphenyl-3-yl-2-methylpyridin-4(1H)-one | HCID 67419356 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09399651B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-20693faa630b4039bf98a16416dd299e |
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| Source note | uspto-grants-2016_07 |
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