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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843877Generated: October 30, 2026

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

https://huagongshe.com/reaction/843877

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 numberUS06380201B1
Source datasetuspto-grants-2002_04
ORD IDord-1db0d8870a94446dbebb76edc28c15fc
Source noteuspto-grants-2002_04