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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777693Generated: October 31, 2026

5-Chloro-1H-indole-3-ethylamine monohydrochloride → N-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-(phenylamino)benzamide

https://huagongshe.com/reaction/1777693

Reaction equation

Participants

RoleNameHCIDCharge
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—
Reactant3-Anilinobenzoic acidHCID 12850341—
SolventDimethylformamideHCID 6228—
ProductN-(2-(5-Chloro-1H-indol-3-yl)ethyl)-3-(phenylamino)benzamideHCID 7145128725.4%

Reaction Steps

A mixture of 3-(phenylamino)benzoic acid (0.155 g, 0.727 mmol), 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.168 g; 0.727 mmol), HATU (0.303 g; 0.799 mmol) and N,N-diisopropylethyldiamine (0.313 mL; 1.82 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 by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.072 g (25%) of the title compound as a pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266832B2
Source datasetuspto-grants-2016_02
ORD IDord-5d68241c1e794885b7e49bb11d5b0282
Source noteuspto-grants-2016_02