HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-nitrobenzenesulfonamide → 2-Cyclopropylamino-5-nitrobenzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-nitrobenzenesulfonamide | HCID 66784 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Cyclopropylamino-5-nitrobenzenesulphonamide | HCID 67530158 | — |
Reaction Steps
2-Chloro-5-nitrobenzenesulphonamide (5 g) prepared in the Step above is introduced into a hermetically closed vessel containing a mixture of dioxane (70 mL) and cyclopropylamine (3.5 mL). The hermetically closed vessel is placed in an oven at 100° C. for 24 hours. After this time period, the solvent and the reagent are removed by concentrating under reduced pressure. The residue is taken up in methanol (20 mL) and the insoluble material, which contains the title product, is collected by filtration, washed with methanol and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741320B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-cc7cdf4d90fc4c72980716ddfe9808c6 |
| Source note | uspto-grants-2010_06 |