HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → N-(1-Benzyl-piperidin-4-yl)-2-chloro-N-isopropyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Benzyl-N-isopropylpiperidin-4-amine | HCID 10728310 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-Benzyl-piperidin-4-yl)-2-chloro-N-isopropyl-acetamide | HCID 66565165 | 50.3% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a mixture of 1-benzyl-4-(isopropylamino)piperidine (8 g, 34.45 mmol) and DIPEA (7.2 mL, 41.3 mmol) in 200 mL of dichloromethane was added dropwise a solution of 2-chloroacetyl chloride (3.01 mL, 37.9 mmol) in dichloromethane (400 mL) at 0° C. The reaction mixture was stirred at 0° C. for 15 min and then at room temperature for 2 h. The reaction mixture was then washed with saturated sodium bicarbonate, brine, dried over magnesium sulfate and concentrated in vacuo. The resulting residue was purified by flash column chromatography (ethyl acetate/hexane/triethylamine: 42.5/56.5/1) to give 5.35 g of the title intermediate as a viscous oil (50% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08080565B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-64ceaa9e27b34369b9ec8a7b788eef19 |
| Source note | uspto-grants-2011_12 |