HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Aminosulfonyl)-5-chlorophthalimide → Phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Aminosulfonyl)-5-chlorophthalimide | HCID 19733 | — |
| Reactant | N,N-Diethylethylenediamine | HCID 60993 | — |
| Reactant | HCID 13473189 | HCID 13473189 | — |
| Product | Phthalimide | HCID 6809 | 50% |
Reaction Steps
6-Chloro-2-[2-(diethylamino)ethyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamide. Reaction of a mixture of 4-chloro-5-sulfamoylphthalimide and 2-(diethylamino)ethylamine according to the procedure of Example 1(a) afforded a 50% yield of the 1,3-dioxoisoindole intermediate. Crystallization of this material from dimethylformamide-ethanol provided analytically pure 6-chloro-2-[2-(diethylamino)ethyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamide, m.p. 152°-154°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505911 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-e5994e838e7c410182031301b6a2c576 |
| Source note | uspto-grants-1985_03 |