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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414411Generated: November 2, 2026

Triethylamine → N-[2-(5-cyano-2-benzyloxyphenoxy)ethyl]-4-(1-t-butoxycarbonyl-4-piperidyloxy)benzamide

https://huagongshe.com/reaction/2414411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-{[1-(tert-Butoxycarbonyl)piperidin-4-yl]oxy}benzoic acidHCID 2794649—
Reactant3-(2-Aminoethoxy)-4-benzyloxybenzonitrile hydrochlorideHCID 22645190—
SolventDimethylformamideHCID 6228—
ProductN-[2-(5-cyano-2-benzyloxyphenoxy)ethyl]-4-(1-t-butoxycarbonyl-4-piperidyloxy)benzamideHCID 22645130—

Reaction Steps

1.06 g (3.50 mmol) of 3-(2-aminoethoxy)-4-benzyloxybenzonitrile hydrochloride was dissolved in 15 ml of DMF. 1.23 g (3.84 mmol) of 4-(1-t-butoxycarbonyl-4-piperidyloxy)benzoic acid, 710 mg (4.2 mmol)) of 2-chloro-1,3-dimethylimidazonium chloride and 1.45 ml (5.19 mmol) of triethylamine were added to the obtained solution, and they were stirred overnight. After the treatment with dichloromethane as the extraction solvent in an ordinary manner, the solvent was evaporated, and the obtained residue was purified by the silica gel column chromatography to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812231B2
Source datasetuspto-grants-2004_11
ORD IDord-4cd977b5d60d4af6b66bab3b76866f2e
Source noteuspto-grants-2004_11