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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130408Generated: October 30, 2026

N-(5-bromo-2-fluorophenyl)acetamide → Ammonia

https://huagongshe.com/reaction/130408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(5-bromo-2-fluorophenyl)acetamideHCID 242827—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactantrel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductAmmoniaHCID 22210%
ProductN-[5-(cis-3,5-Dimethyl-1-piperazinyl)-2-fluorophenyl]acetamideHCID 69198003—

Reaction Steps

The product of Step 1 (5.12 g, 18.7 mmol), cis-2,6-dimethyl piperazine (3.20 g, 28.1 mmol), sodium tert-butoxide (5.39 g, 56.1 mmol), tris(dibenzylideneacetone)dipalladium(0) (343 mg, 0.37 mmol) and 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (444 mg, 1.12 mmol) were heated at reflux for 16 hours in 1,4-dioxane (50 ml). The solution was filtered through celite washing through with ethyl acetate. The filtrate was concentrated in vacuo, and the residue partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic phase was washed with water, 50% saturated brine solution, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel (ethyl acetate, then a gradient of dichloromethane to 10% 2M methanolic ammonia in dichloromethane) to afford the title compound. MS (ES+) m/e 266 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-b822db0c06684382beca792c1e828e8f
Source noteuspto-grants-2008_06