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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | rel-(2R,6S)-2,6-dimethylpiperazine | HCID 6950261 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 2-Chloro-5-iodoaniline | HCID 39871971 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroaniline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07381728B2 |
|---|
| Source dataset | uspto-grants-2008_06 |
|---|
| ORD ID | ord-44e8e96a685b488caef2e86be63d9b64 |
|---|
| Source note | uspto-grants-2008_06 |
|---|