HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-butyl N-[1-(dimethylsulfamoyl)piperidin-4-yl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-[1-(dimethylsulfamoyl)piperidin-4-yl]carbamate | HCID 47215822 | 85% |
Reaction Steps
To a solution of 412 mg (2.06 mmol) of tert-butyl 4-piperidinyl-carbamate in 20 mL of dichloromethane were added 430 μL (3.09 mmol) of triethylamine and 265 μL (2.47 mmol) of dimethylsulfamoyl chloride and the mixture was stirred for 2 hours at room temperature. Then, the mixture was treated with ethyl acetate and the organic layer was washed with water and saturated saline solution, and then, dried over with anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography (eluent:dichloromethane/methanol=40/1) to give 536 mg (85%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932250B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-93eb03f1f04c42b5821370c8b0d0a233 |
| Source note | uspto-grants-2011_04 |