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 | 3-Pyridinemethanamine | HCID 31018 | — |
| Reactant | HCID 13473184 | HCID 13473184 | — |
| Product | Phthalimide | HCID 6809 | 73% |
Reaction Steps
6-Chloro-2,3-dihydro-1,3-dioxo-2-(3-pyridinylmethyl)-1H-isoindole-5-sulfonamide. Reaction of a mixture of 4-chloro-5-sulfamoylphthalimide and 3-(aminomethyl)pyridine according to the procedure of Example 1(a) afforded a 73% yield of the 1,3-dioxoisoindole intermediate. Crystallization of this material from dimethylformamide-methanol provided analytically pure 6-chloro-2,3-dihydro-1,3-dioxo-2-(3-pyridinylmethyl)-1H-isoindole-5-sulfonamide, m.p. 210°-212°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04505911 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-d6881510d7614c218ff40627ed620436 |
| Source note | uspto-grants-1985_03 |