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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069113Generated: October 29, 2026

Water → N-(4-(4-Aminonaphthalen-1-yloxy)pyridin-2-yl)-2-methoxyacetamide

https://huagongshe.com/reaction/2069113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Methoxy-N-(4-(4-nitronaphthalen-1-yloxy)pyridin-2-yl)acetamideHCID 67452476—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
ProductN-(4-(4-Aminonaphthalen-1-yloxy)pyridin-2-yl)-2-methoxyacetamideHCID 66718180—

Reaction Steps

To a solution of 2-methoxy-N-(4-(4-nitronaphthalen-1-yloxy)pyridin-2-yl)acetamide (50.0 g, 142 mmol) in DMF (500 mL) under nitrogen was added palladium on carbon (10% w/w Pd/C, 5.0 g, 14.15 mmol) and the mixture was purged with hydrogen and maintained under a slight positive hydrogen atmosphere for 48 hr. The catalyst was removed by filtration through celite and the pad washed with DMF (2×100 mL) and then DCM (100 mL). The solvents were removed in vacuo to afford a dark brown residue which was treated with water (150 mL) and the mixture evaporated. Toluene (100 mL) was added and evaporated to remove residual water. After drying overnight under vacuum, the material was triturated from diethyl ether (250 mL) to give the title compound, Intermediate B1, as a green solid (43.3 g, 85%): m/z 324 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299074B2
Source datasetuspto-grants-2012_10
ORD IDord-5c25203ae55e4d77bac68aec664728e2
Source noteuspto-grants-2012_10