HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Benzylnormechlorethamine → N-(Phenylmethyl)-1-piperidinesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Benzylnormechlorethamine | HCID 5928 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 178486263 | HCID 178486263 | — |
| Product | N-(Phenylmethyl)-1-piperidinesulfonamide | HCID 2989594 | 52% |
Reaction Steps
To a solution of the methylene sulfonamide from part F (20.46 g, 51.5 mmol) in dimethylformamide (90 mL) was added potassium carbonate (21.3 g, 154.7 mmol), bis-(2-chloroethyl)benzyl amine (12.0 g, 51.5 mmol; and 18-Crown-6 (700 mg). The slurry was stirred at sixty degrees Celsius. After twenty four hours the reaction was concentrated in vacuo. The residue was taken up in ethyl acetate, washed with water three times, saturated sodium chloride solution, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was recrystallized (methanol) to give the N-benzyl piperidine sulfonamide as a white solid (15 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800646B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-8dc305dd32d7485badcabecd3c380c4b |
| Source note | uspto-grants-2004_10 |