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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737828Generated: November 2, 2026

Triethylamine → 4-fluoro-N-(1H-indol-5-yl)benzamide

https://huagongshe.com/reaction/1737828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant5-AminoindoleHCID 78867—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-fluoro-N-(1H-indol-5-yl)benzamideHCID 281450684%

Reaction Steps

To a solution of 3.96 gm (30.0 mMol) 5-amino-1H-indole in 150 mL tetrahydrofuran were added 5.6 mL triethylamine followed by a solution of 5.2 gm (33.0 mMol) 4-fluorobenzoyl chloride in 30 mL tetrahydrofuran. After 18 hours the reaction mixture was poured into water, made basic with sodium hydroxide solution, and extracted with dichloromethane. The organic extracts were combined, dried over sodium sulfate and concentrated under reduced pressure to give a purple solid. This residue was recrystallized from ethyl acetate/hexane to give 6.37 gm (84%) 5-(4-fluoro-benzoyl)amino-1H-indole as brown crystals in two crops.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962474
Source datasetuspto-grants-1999_10
ORD IDord-909e0b37bb294666997fc1b3c6500c71
Source noteuspto-grants-1999_10