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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691607Generated: October 26, 2026

Ammonia → 5-Fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1691607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantThionyl ChlorideHCID 24386—
Reactant5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acidHCID 57431513—
SolventTolueneHCID 1140—
Product5-Fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 6684569629.1%

Reaction Steps

A suspension, stirred at 20° C., of 2 g (6.96 mmol) of 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylic acid, prepared according to the protocol described in step 1.1, in 80 ml of dry toluene is admixed with 5.08 ml (69.62 mmol) of thionyl chloride. The reaction mixture is stirred at reflux for 2 hours and then concentrated under reduced pressure. The resulting product is taken up in 10 ml of dichloromethane and this solution is poured dropwise into a solution of 9.12 ml (69.62 mmol) of 30% aqueous ammonia. The reaction mixture is stirred at 20° C. for 14 hours. After this time a solid is recovered by filtration and triturated in 50 ml of diisopropyl ether. Filtration and drying under reduced pressure give 0.58 g of expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153796B2
Source datasetuspto-grants-2012_04
ORD IDord-fa6bd15c00ac4b898eb0f8846c2add89
Source noteuspto-grants-2012_04