HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butylamine → N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | 4-[2-(-1-Oxo-isoindoline-2-carboxamido)ethyl]-benzenesulfonyl-urea | HCID 70578684 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea | HCID 21162325 | — |
Reaction Steps
4 g of N-(4-[2-(-1-oxo-isoindoline-2-carboxamido)ethyl]-benzenesulfonyl-urea (melting point 207°-209° C., prepared from 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonamide and potassium cyanate in 80% ethanol) and 0.73 g of butylamine in 100 ml of dioxane are refluxed for 1 hour. The solvent is then distilled off under reduced pressure, the residue is reprecipitated from very dilute ammonia and recrystallized from dilute acetone. The N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl urea obtained melts at 188° to 190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282239 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-db1a032d292e415ca0c468f847e11b59 |
| Source note | uspto-grants-1981_08 |