HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → N,N-dimethylpiperidine-4-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzyl 4-(chlorosulfonyl)piperidine-1-carboxylate | HCID 21931260 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-dimethylpiperidine-4-sulfonamide | HCID 46779214 | 133.3% |
Reaction Steps
A suspension of an amine such as dimethylamine (4.72 mmol) and sodium hydride (4.72 mmol) in N,N-dimethylformamide (10 ml) was stirred for five minutes at room temperature. Then phenylmethyl 4-(chlorosulfonyl)-1-piperidinecarboxylate (1.60 mmol) was added to the reaction mixture and stirred at 100° C. for 3 hours. The reaction mixture was poured into water (25 ml) and extracted with ethyl acetate (3×25 ml). The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated to give the title compound (410 mg, 80% yield) as an off-white solid. MS(ES)+ m/e 327.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592342B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-26b17b507f674f7b811e61d47f6ef344 |
| Source note | uspto-grants-2009_09 |