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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610293Generated: October 30, 2026

1-Naphthalenecarbonyl chloride → N-((1RS,2SR)-2-(4-fluorophenyl)-2-hydroxy-1-((4-(methyloxy)phenyl)methyl)ethyl)-1-naphthalenecarboxamide

https://huagongshe.com/reaction/1610293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Naphthalenecarbonyl chlorideHCID 70146—
ReactantSodium BicarbonateHCID 516892—
Reactant(1RS,2SR)-2-amino-1-(4-fluorophenyl)-3-(4-(methyloxy)phenyl)-1-propanolHCID 22261918—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-((1RS,2SR)-2-(4-fluorophenyl)-2-hydroxy-1-((4-(methyloxy)phenyl)methyl)ethyl)-1-naphthalenecarboxamideHCID 2226166389%

Reaction Steps

To a solution of (1RS,2SR)-2-amino-1-(4-fluorophenyl)-3-(4-(methyloxy)phenyl)-1-propanol (450 mg, 1.64 mmol) in ethyl acetate (15 ml) were added 1-naphthoyl chloride (369 ml, 2.45 mmol) and saturated aqueous sodium hydrogen carbonate (15 ml) and the mixture was stirred overnight at room temperature. The reaction solution was diluted with water (100 ml) and extracted with ethyl acetate (100 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was recrystallized from ethyl acetate-hexane to give the title compound (622 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-0a2d0bc3b8024ce697a95559b557aadd
Source noteuspto-grants-2006_01