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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164543Generated: October 31, 2026

4-(Aminosulfonyl)-5-chlorophthalimide → Phthalimide

https://huagongshe.com/reaction/2164543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminosulfonyl)-5-chlorophthalimideHCID 19733—
Reactant2-PyridineethanamineHCID 75919—
ReactantHCID 13473185HCID 13473185—
ProductPhthalimideHCID 680981%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505911
Source datasetuspto-grants-1985_03
ORD IDord-267079d03c60444da0694c351eb73e29
Source noteuspto-grants-1985_03