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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747492Generated: November 2, 2026

Ammonium Chloride → HCID 60701687, compound

https://huagongshe.com/reaction/1747492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Bromo-3-chloropyridineHCID 7016326—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 60701687HCID 6070168739%

Reaction Steps

Sodium tert-butoxide (0.936 g, 9.74 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.364 g, 0.585 mmol), and tris(dibenzylideneacetone)dipalladium(0) (0.178 g, 0.195 mmol) were added to a solution of ethyl piperidine-4-carboxylate (2.45 g, 15.6 mmol) and 2-bromo-3-chloropyridine (1.50 g, 7.79 mmol) in toluene (30 mL) under a nitrogen atmosphere, and the mixture was stirred for 4 hours under heating to reflux. A saturated ammonium chloride aqueous solution was added to the reaction solution, followed by extraction with ethyl acetate twice. The obtained organic layer was washed with brine and then dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography [elute: hexane/ethyl acetate=90/10] to obtain the title compound (0.813 g, yield: 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150575B2
Source datasetuspto-grants-2015_10
ORD IDord-6131b781e7c64440bc1dc73787f9ed08
Source noteuspto-grants-2015_10