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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911241Generated: October 26, 2026

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

https://huagongshe.com/reaction/1911241

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 66845696—

Reaction Steps

To a suspension, stirred at 20° C., of 2 g (6.96 mmol) of 5-fluoro-1-[(3-fluorophenyl)-methyl]-1H-indole-2-carboxylic acid, prepared in step 1.1, in 80 mL of dry toluene are added 5.08 mL (69.62 mmol) of thionyl chloride. The reaction mixture is stirred for 2 hours at reflux and is 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 for 14 hours at 20° C. After this time, a solid is collected by filtration, and is triturated in 50 mL of diisopropyl ether. After filtering off and drying under reduced pressure, 0.58 g of the expected product is collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604050B2
Source datasetuspto-grants-2013_12
ORD IDord-926c10d13e394d7e964636bf702a7467
Source noteuspto-grants-2013_12