HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetylsulfanilyl chloride → N-{4-[(1-Butylpiperidin-4-yl)sulfamoyl]phenyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Butylpiperidin-4-amine | HCID 12262820 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-{4-[(1-Butylpiperidin-4-yl)sulfamoyl]phenyl}acetamide | HCID 21563541 | — |
Reaction Steps
7.0 Grams of N-acetylsulphanilyl chloride were added in portions to a stirred, ice cooled, mixture of 4.7 grams of 4-amino-1-n-butyl piperidine and 6.3 grams of sodium bicarbonate in 75 milliliters of water and 35 milliliters of chloroform. After stirring overnight at room temperature the mixture was filtered, washed with water, and dried to give 4.2 grams of the title compound. Melting Point 174°-175°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03933829 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-9affc9fbd6fb42b2a10829af12de4f92 |
| Source note | uspto-grants-1976_01 |