HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | N-Butyl-N'-hydroxyurea | HCID 79761 | — |
| Reactant | 4-[2-(1-Oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfinic acid | HCID 21162398 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea | HCID 21162325 | — |
Reaction Steps
3.4 g of 4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfinic acid (crude product, prepared by reduction of the sulfochloride with sodium sulfite) and 1.4 g of N-hydroxy-N'-butyl-urea are suspended in 40 ml of dioxane and a solution of 1 ml of thionyl chloride in 10 ml of dioxane is added dropwise while stirring. The mixture is then heated for 2 hours to 60° C., whereby a limpid solution is formed. The solution is poured into water, the precipitated substance is treated with dilute ammonia, filtered, acidified and the reaction product is recrystallized from dilute acetone. The N-(4-[2-(1-oxo-isoindoline-2-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl-urea obtained melts at 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282239 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-2a951a18b4854d6ea0a8d51dfe41047f |
| Source note | uspto-grants-1981_08 |