HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215755Generated: October 31, 2026
N-Acetylsulfanilyl chloride → N-(4-{[3-(morpholin-4-yl)propyl]sulfamoyl}phenyl)acetamide
https://huagongshe.com/reaction/215755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-Aminopropyl)morpholine | HCID 61055 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-{[3-(morpholin-4-yl)propyl]sulfamoyl}phenyl)acetamide | HCID 2144799 | 62% |
Reaction Steps
To the solution of 2.8 g (0.020 mol) of 3-morpholinopropylamine in 15 ml of acetone, the solution of 3.3 g (0.024 mol) of potassium carbonate in 3 ml of water was added under stirring. To this mixture, 5 g (0.021 mol) of 4-acetamidobenzenesulphonyl chloride XII was added portionwise at the room temperature for 15 min. The mixture was then stirred at the room temperature for another 2 hours. One half of the solvent volume was distilled off from the mixture, the mixture was cooled to 0° C., Obtained solid was separated, washed 3 times with 5 ml of ice water and dried. Afforded 4.2 g (62%) of 4-acetamido-N-(3-morpholinopropyl)benzenesulphonamide XIII, colourless solid, m.p. 97-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193184B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-3dbe52c20a23496593af253c0ba69a6d |
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| Source note | uspto-grants-2012_06 |
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