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 | 4-Pyridineethanamine | HCID 83275 | — |
| Reactant | HCID 13473186 | HCID 13473186 | — |
| Product | Phthalimide | HCID 6809 | 93% |
Reaction Steps
6-Chloro-2,3-dihydro-1,3-dioxo-2-[2-(4-pyridinyl)ethyl]-1H-isoindole-5-sulfonamide. Reaction of a mixture of 4-chloro-5-sulfamoylphthalimide and 4-(2-aminoethyl)pyridine according to the procedure of Example 1(a) afforded a 93% yield of the 1,3-dioxoisoindole intermediate. Crystallization of this material from dimethylformamide provided analytically pure 6-chloro-2,3-dihydro-1,3-dioxo-2-[2-(4-pyridinyl)ethyl]-1H-isoindole-5-sulfonamide, m.p. 277°-278° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505911 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-891346c68e6f44fba9d4c1eeac3bac32 |
| Source note | uspto-grants-1985_03 |