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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945370Generated: October 27, 2026

Ethyl 3-aminobenzoate → 3-[2-(4-Adamantan-1-yl-phenoxy)-acetylamino]-benzoic acid ethyl ester

https://huagongshe.com/reaction/1945370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-aminobenzoateHCID 11400—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantPMID26882240-Compound-8HCID 625381—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
Product3-[2-(4-Adamantan-1-yl-phenoxy)-acetylamino]-benzoic acid ethyl esterHCID 2481089489.7%

Reaction Steps

To a mixture of [4-(1-adamantyl)phenoxy]acetic acid (143.2 mg, 0.5 mmol), 3-aminobenzoic acid ethyl ester (123.9 mg, 0.5 mmol), N-(3-dimethylaminopropyl)-N′-ethyl carbodiimide HCl (EDC) (143.8 mg, 0.75 mmol) and 1-hydroxybenzotriazole (HOBt) (101.4 mg, 0.75 mmol) in DMF (6 mL) was added N,N-diisopropylethylamine, redistilled (DIPEA) (97.0 mg, 0.13 mL, 0.75 mmol). The mixture wag stirred overnight, and then partitioned between ethyl acetate and 10% HCl. The organic phase was washed with brine, dried (MgSO4 anh), and concentrated. The residue was purified by silica gel flash column chromatography (n-Hexane:Ethyl acetate:MeOH=6:3:1) to give 3-[2-(4-adamantan-1-yl-phenoxy)-acetylamino]-benzoic acid ethyl ester as a white solid (194.4 mg, 89.7% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394799B2
Source datasetuspto-grants-2013_03
ORD IDord-fd6b237e901545e893a67bc1978ab111
Source noteuspto-grants-2013_03