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 | 2-Pyridineethanamine | HCID 75919 | — |
| Reactant | HCID 13473185 | HCID 13473185 | — |
| Product | Phthalimide | HCID 6809 | 81% |
Reaction Steps
6-Chloro-2,3-dihydro-1,3-dioxo-2-[2-(2-pyridinyl)ethyl]-1H-isoindole-5-sulfonamide. Reaction of a mixture of 4-chloro-5-sulfamoylphthalimide and 2-(2-aminoethyl)pyridine according to the procedure of Example 1(a) afforded 81% yield of the 1,3-dioxoisoindole intermediate. Crystallization of this material from dimethylformamidemethanol provided analytically pure 6-chloro-2,3-dihydro-1,3-dioxo-2-[2-(2-pyridinyl)ethyl]-1H-isoindole-5-sulfonamide, m.p. 240°-241°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505911 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-267079d03c60444da0694c351eb73e29 |
| Source note | uspto-grants-1985_03 |