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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207172Generated: November 1, 2026

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

https://huagongshe.com/reaction/2207172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-4-(6-methoxy-1-oxo-tetralin-2-yl)but-2-enalHCID 90303875—
Reactant4-[[3-(Trifluoromethyl)phenyl]methylamino]but-3-en-2-oneHCID 131735883—
Product2-[[3-acetyl-1-[[3-(trifluoromethyl)phenyl]methyl]-4H-pyridin-4-yl]methyl]-6-methoxy-tetralin-1-oneHCID 118557871—

Reaction Steps

The title compound 65 is prepared according to the procedure reported in step D of Example 8 with aldehyde 54 (100 mg, 0.41 mmol) and enamine 66 (100 mg, 0.41 mmol) as reactants. Purification by column chromatography on SiO2 (Petroleum Ether/EtOAc=2:1) afford the title compound 65 as a pale yellow solid. (Yield 65 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376387B2
Source datasetuspto-grants-2016_06
ORD IDord-174e380100c84c0c83f399a1afdb5d65
Source noteuspto-grants-2016_06