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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207170Generated: October 31, 2026

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

https://huagongshe.com/reaction/2207170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-4-(6-methoxy-1-oxo-tetralin-2-yl)but-2-enalHCID 90303875—
Reactant4-[(3-Chlorophenyl)methylamino]but-3-en-2-oneHCID 131735882—
Product2-[[3-acetyl-1-[(3-chlorophenyl)methyl]-4H-pyridin-4-yl]methyl]-6-methoxy-tetralin-1-oneHCID 118558039—

Reaction Steps

The title compound 63 is prepared according to the procedure reported in step D of Example 8 with aldehyde 54 (100 mg, 0.41 mmol) and enamine 64 (90 mg, 0.42 mmol) as reactants. Purification by column chromatography on SiO2 (Petroleum Ether/EtOAc=2:1) afford the title compound 63 as a yellow solid. (Yield 70 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376387B2
Source datasetuspto-grants-2016_06
ORD IDord-2d638abf508646b1a3657f1aca106e54
Source noteuspto-grants-2016_06