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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466229Generated: November 1, 2026

Potassium Carbonate → N-[4-(2-tert-butoxy-pyridin-4-yl)-benzyl]-2,6-dichloro-benzamide

https://huagongshe.com/reaction/1466229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-tert-butoxypyridineHCID 45787872—
Reactant4-[(2,6-Dichloro-benzoylamino)methyl]phenylboronic acidHCID 71149972—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventDimethylformamideHCID 6228—
ProductN-[4-(2-tert-butoxy-pyridin-4-yl)-benzyl]-2,6-dichloro-benzamideHCID 71149992—

Reaction Steps

4-[(2,6-Dichloro-benzoylamino)methyl]phenylboronic acid (5 g, 15.4 mmol), potassium carbonate (5 g), and [1,1′bis(diphenylphosphino)ferrocene]dichloropalladium (II) (0.56 g, 0.77 mmol) were combined in a round bottom flask. 4-Bromo-2-(t-butoxy) pyridine (3.55 g, 15.4 mmol) was dissolved in 20 mL DMF and added to the flask under stirring. The flask was flushed with nitrogen and 10 mL water was added. The reaction mixture was stirred at 70° C. for two hours. After cooling the mixture was poured into 300 mL ethyl acetate and washed with water and brine. The organic phase was dried with magnesium sulfate and evaporated under vacuum. The crude N-[4-(2-tert-butoxy-pyridin-4-yl)-benzyl]-2,6-dichloro-benzamide was further purified by silica gel chromatography (eluent: hexone/ethyl acetate 1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000015B2
Source datasetuspto-grants-2015_04
ORD IDord-82ad8f7b498741238ff3fc5ce7ba84c1
Source noteuspto-grants-2015_04