HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → Acetamide, N-(4-((methylamino)sulfonyl)phenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Product | Acetamide, N-(4-((methylamino)sulfonyl)phenyl)- | HCID 145971 | — |
Reaction Steps
10.5 g (45 mmol) of 4-acetylaminobenzenesulfonyl chloride are stirred at 50° C. for 3 hours in 100 ml of 40% strength methylamine solution. The solution is then extracted three times with ethyl acetate. The organic phases are dried using Na2SO4 and concentrated. The residue is stirred with dichloromethane and the insoluble constituents are filtered off. Concentration of the filtrate gives the desired sulfonamide in adequate purity and almost quantitative yield. (MS-CI+: 229.1; LCMS Rt=3.249 min)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399824B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-35c085e3d4c14db29cd37a7023702cfa |
| Source note | uspto-grants-2002_06 |