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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945401Generated: October 27, 2026

Methanone, (3-aminophenyl)phenyl- → 2-(4-Adamantan-1-yl-phenoxy)-N-(3-benzoyl-phenyl)-acetamide

https://huagongshe.com/reaction/1945401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanone, (3-aminophenyl)phenyl-HCID 17817—
ReactantDiisopropylethylamineHCID 81531—
ReactantPMID26882240-Compound-8HCID 625381—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantEthylcarbodiimide hydrochlorideHCID 21883477—
SolventDimethylformamideHCID 6228—
Product2-(4-Adamantan-1-yl-phenoxy)-N-(3-benzoyl-phenyl)-acetamideHCID 2481132774.4%

Reaction Steps

To a solution of the (4-adamantan-1-yl-phenoxy)-acetic acid (143 mg, 0.5 mmol) and (3-amino-phenyl)phenyl-methanone (148 mg, 0.75 mmol) in DMF (5.0 mL) were added 1-[3-dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (EDC) (144.0 mg, 0.75 mmol), 1-hydroxybenzotriazole hydrate (HOBT) (101 mg, 0.75 mmol), and N,N-diisopropylethylamine (DIPEA) (0.13 ml, 0.75 mmol). The reaction mixture was stirred at room temperature overnight, and then partitioned between ethyl acetate and brine. The organic phase was dried (MgSO4 anh), and concentrated. Purification by silica gel column chromatography (n-Hexane:EtOAc:MeOH=12:3:1) gave 2-(4-Adamantan-1-yl-phenoxy)-N-(3-benzoyl-phenyl)-acetamide as a white solid (173.1 mg, 74.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394799B2
Source datasetuspto-grants-2013_03
ORD IDord-79ee9062cdb946c79e4a3a5129e69a89
Source noteuspto-grants-2013_03