Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610637Generated: October 26, 2026

5-Chloro-1-naphthoic acid → N-[(1RS,2SR)-1-(4-tert-butoxybenzyl)-2-(3-chlorophenyl)-2-hydroxyethyl]-5-chloro-1-naphthamide

https://huagongshe.com/reaction/1610637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1-naphthoic acidHCID 937057—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(1RS,2SR)-2-amino-3-(4-tert-butoxyphenyl)-1-(3-chlorophenyl)propan-1-olHCID 22261849—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-[(1RS,2SR)-1-(4-tert-butoxybenzyl)-2-(3-chlorophenyl)-2-hydroxyethyl]-5-chloro-1-naphthamideHCID 22261909—

Reaction Steps

To a solution of (1RS,2SR)-2-amino-3-(4-tert-butoxyphenyl)-1-(3-chlorophenyl)propan-1-ol (300 mg, 0.90 mmol) in acetonitrile (20 ml) were added 5-chloronaphthalenecarboxylic acid (186 mg, 0.90 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (258 mg, 1.35 mmol) and 1-hydroxybenzotriazole hydrate (138 mg, 0.90 mmol), 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 successively with water and saturated brine, dried (anhydrous magnesium sulfate) and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1-2:1). Recrystallization from ethyl acetate-hexane gave the objective substance (136 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-0600c27278354b4ea330db4f0ec0a641
Source noteuspto-grants-2006_01