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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398495Generated: October 29, 2026

N-(5-benzyloxy-pyridin-2-yl)-3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionamide → 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(5-hydroxy-pyridin-2-yl)-propionamide

https://huagongshe.com/reaction/398495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-benzyloxy-pyridin-2-yl)-3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionamideHCID 22315199—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(5-hydroxy-pyridin-2-yl)-propionamideHCID 2231511981%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of N-(5-benzyloxy-pyridin-2-yl)-3-cyclopentyl-2-(3,4-dichloro-phenyl)-propionamide (145.3 mg, 0.3 mmol) in methanol (5.1 mL) was treated with 10% palladium on activated carbon. The reaction mixture was stirred under hydrogen gas at 25° C. for 16 h. The catalyst was then filtered off through a pad of celite, which was washed well with ethyl acetate. The resulting filtrate was concentrated in vacuo to give 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(5-hydroxy-pyridin-2-yl)-propionamide (92.2 mg, 78.5%) as a tan solid: mp 79-81° C.; EI-HRMS m/e calcd for C19H20Cl2N2O2 (M+) 378.0896, found 378.0890.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-ebdfe815893b41e98f8fdf41e0ccb107
Source noteuspto-grants-2003_08