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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777694Generated: November 1, 2026

3-Phenoxybenzoic acid → N-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-phenoxybenzamide

https://huagongshe.com/reaction/1777694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenoxybenzoic acidHCID 19539—
Reactant5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDimethylformamideHCID 6228—
ProductN-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-phenoxybenzamideHCID 6797369719%

Reaction Steps

A mixture of 3-phenoxybenzoic acid (0.200 g, 0.934 mmol), 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.215 g; 0.934 mmol), HATU (0.389 g; 1.03 mmol) and N,N-diisopropylethyldiamine (0.402 mL; 2.33 mmol) in DMF (5 mL), was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and sodium hydrogen sulphate, the organic layer was washed with sodium carbonate, brine, dried and concentrated in vacuo. The crude mixture was purified twice by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.068 g (19%) of the title compound as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266832B2
Source datasetuspto-grants-2016_02
ORD IDord-076f60cca563439a82b415b9e098e971
Source noteuspto-grants-2016_02