Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506503Generated: November 2, 2026

Water → N-[6-chloropyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamide

https://huagongshe.com/reaction/506503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-Amino-2-chloropyridineHCID 79305—
ReactantTrimethylaluminumHCID 16682925—
ReactantEthyl 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylateHCID 57431514—
SolventTolueneHCID 1140—
ProductN-[6-chloropyridin-3-yl]-5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxamideHCID 86631224—

Reaction Conditions

Temperature0 °C

Reaction Steps

23.8 ml (47.57 mmol) of a 2M solution of trimethylaluminum in toluene are added to a solution, stirred at 20° C. under an argon atmosphere, of 4.48 g (34.89 mmol) of 6-chloro-3-aminopyridine in 317 ml of toluene. The solution is then brought to 120° C. and 10 g (31.71 mmol) of ethyl 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylate are added in several steps (WO 2006/024776). The reaction mixture is refluxed for 4 hours and is then cooled to 0° C. 15 ml of water are added to the reaction medium, which is then extracted with twice 200 ml of ethyl acetate. The organic phases are combined and washed twice with 50 ml of water and once with 50 ml of a saturated sodium chloride solution, and then dried over magnesium sulfate and concentrated under reduced pressure. The residue obtained is triturated in 100 ml of ethyl ether, the product is filtered, and 10 g of expected product are recovered in the form of a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786104B2
Source datasetuspto-grants-2010_08
ORD IDord-247ecf90b93940208ba4c1c785a2a5d6
Source noteuspto-grants-2010_08