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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454575Generated: October 30, 2026

Methyl 2-(2-(benzyloxy)-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate → Methyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate

https://huagongshe.com/reaction/454575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(2-(benzyloxy)-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoateHCID 66990524—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductMethyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoateHCID 5850886781.1%

Reaction Steps

To a methanol (3.0 mL) solution of the obtained methyl 2-(2-(benzyloxy)-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate (0.086 g), 10% palladium-carbon (43 mg) was added, followed by stirring under a hydrogen atmosphere at room temperature for 2 hours and 10 minutes. The insoluble substance was removed by filtration, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the obtained residue, and the solid substance was collected by filtration to obtain 0.058 g of methyl 2-(2-hydroxy-5-(1-methylpiperidin-4-yl)benzamido)-4-phenylbenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-b55e1bce4cc1451f8b3bfd4e633fe9b5
Source noteuspto-grants-2013_07