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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130422Generated: October 26, 2026

Methane → 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroaniline

https://huagongshe.com/reaction/130422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactantrel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
ReactantSodium t-butoxideHCID 23676156—
Reactant2-Chloro-5-iodoanilineHCID 39871971—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroanilineHCID 59007078—

Reaction Steps

2-Chloro-5-iodoaniline (630 mg, 2.49 mmol) was heated at reflux in acetic acid (7 ml) and acetic anhydride (7 ml) for 18 hours. The solution was concentrated in vacuo, azeotroping with toluene. The residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic phase separated and washed with saturated aqueous sodium bicarbonate solution, water, brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to afford a mixture of the mono- and di-acylated acetamide (N-(2-chloro-5-iodophenyl)acetamide and N-acetyl-N-(2-chloro-5-iodophenyl)acetamide). To this product (820 mg) in 1,4-dioxane (12 ml) was added cis-2,6-dimethyl piperazine (416 mg, 3.64 mmol), sodium tert-butoxide (700 mg, 7.29 mmol), tris(dibenzylideneacetone)dipalladium(0) (45 mg, 0.049 mmol) and 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (39 mg, 0.098 mmol) and the reaction heated at reflux for 18 hours under argon. The reaction mixture was cooled, diluted with ethyl acetate (30 ml) and stirred with a mixture of celite and charcoal. The solution was filtered through celite washing 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 treated with 5N HCl (20 ml) and heated at reflux for 24 hours under argon. The reaction was cooled, and the solution washed with ethyl acetate (×3), poured onto ice, basified with 0.880 ammonia and extracted with dichloromethane (×4). The combined extracts were washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel (gradient of 2% to 10% methanol in dichloromethane) to afford the title compound (D34). MS (ES+) m/e 240/242 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381728B2
Source datasetuspto-grants-2008_06
ORD IDord-44e8e96a685b488caef2e86be63d9b64
Source noteuspto-grants-2008_06