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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70339Generated: October 29, 2026

Triethylamine → 3'-({2-[(4,4-Dimethylcyclohexyl)amino]ethyl}oxy)-4-biphenylcarboxamide hydrochloride

https://huagongshe.com/reaction/70339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4,4-Dimethylcyclohexanamine hydrochlorideHCID 24191928—
Reactant3'-[(2-Bromoethyl)oxy]-4-biphenylcarboxamideHCID 58276262—
Reactant3'-[(2-Chloroethyl)oxy]-4-biphenylcarboxamideHCID 58276352—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product3'-({2-[(4,4-Dimethylcyclohexyl)amino]ethyl}oxy)-4-biphenylcarboxamide hydrochlorideHCID 67160430—

Reaction Steps

A mixture of 3′-[(2-chloroethyl)oxy]-4-biphenylcarboxamide and 3′-[(2-bromoethyl)oxy]-4-biphenylcarboxamide (Example II-1) (0.15 g), 4,4-dimethylcyclohexylamine hydrochloride (0.13 g, 0.8 mmol) (prepared according to J. Med. Chem. 1971, 14, p. 600-614) and triethylamine (0.14 g, 1.35 mmol) in methanol (2 mL) was placed in a microwave at 160° C. until the reaction was complete as monitored by LC/MS. The reaction mixture was poured into ethyl acetate and washed several times with 5% Na2CO3 (aq). Silica gel was added to the organic phase and the mixture was concentrated in vacuo. The residue was purified by silica gel chromatography. The fractions containing the desired product were combined and concentrated in vacuo. Dissolved the residue in ethanol, added 1.0N HCl in Et2O until acidic, added ethyl ether until turbid and let stand at room temperature. The resulting solid was filtered, washed with ethyl ether and dried to give 3′-({2-[(4,4-dimethylcyclohexyl)amino]ethyl}oxy)-4-biphenylcarboxamide hydrochloride as an off-white solid. (M+H) 367, 1.83 min. (LC/MS method A)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822518B2
Source datasetuspto-grants-2014_09
ORD IDord-31192e4280154abaa3955ea51a10d8f0
Source noteuspto-grants-2014_09