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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726076Generated: October 30, 2026

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

https://huagongshe.com/reaction/726076

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 numberUS05708008
Source datasetuspto-grants-1998_01
ORD IDord-7cd742c051dd48b2b3df14f496807fef
Source noteuspto-grants-1998_01