HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-{[3-(morpholin-4-yl)propyl]sulfamoyl}phenyl)acetamide → 4-amino-N-[3-(morpholin-4-yl)propyl]benzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-{[3-(morpholin-4-yl)propyl]sulfamoyl}phenyl)acetamide | HCID 2144799 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-amino-N-[3-(morpholin-4-yl)propyl]benzene-1-sulfonamide | HCID 4962821 | 701.4% |
Reaction Steps
The mixture of 3.4 g (0.001 mol) of 4-acetamido-N-(3-morpholinopropyl)benzene sulphonamide XIII and 4 ml of 17% acid was heated for 3.5 hours until slight boiling under stirring. The mixture was cooled to the room temperature and neutralized to chloroform. The solvent was distilled off from the solution and the distillation residue-oil was macerated with ether. Afforded 2.1 g of (71%) 4-amino-N-(3-morpholinopropyl)benzenesulphonamide XIV. Colourless solid, m.p. 96-97° C. Lit. [8] reports 95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193184B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-cc1d299921224b4da6ce8c4a34d72e91 |
| Source note | uspto-grants-2012_06 |