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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207162Generated: October 31, 2026

(E)-4-(6-methoxy-1-oxo-tetralin-2-yl)but-2-enal → 2-[[3-acetyl-1-[(2-fluorophenyl)methyl]-4H-pyridin-4-yl]methyl]-6-methoxy-tetralin-1-one

https://huagongshe.com/reaction/2207162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-4-(6-methoxy-1-oxo-tetralin-2-yl)but-2-enalHCID 90303875—
Reactant4-[(2-Fluorophenyl)methylamino]but-3-en-2-oneHCID 131735881—
Product2-[[3-acetyl-1-[(2-fluorophenyl)methyl]-4H-pyridin-4-yl]methyl]-6-methoxy-tetralin-1-oneHCID 118557974—

Reaction Steps

The title compound 55 is prepared according to the procedure reported in step D of Example 8 with aldehyde 54 (100 mg, 0.41 mmol) and enamine 56 (115 mg, 0.59 mmol) as reactants. Purification by column chromatography on SiO2 (Petroleum/EtOAc=2:1) afford the title compound 55 as a yellow solid. (Yield 0.11 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376387B2
Source datasetuspto-grants-2016_06
ORD IDord-861e2957fe95447e9187387ff8815b8f
Source noteuspto-grants-2016_06