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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164544Generated: October 30, 2026

4-(Aminosulfonyl)-5-chlorophthalimide → Phthalimide

https://huagongshe.com/reaction/2164544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminosulfonyl)-5-chlorophthalimideHCID 19733—
Reactant4-PyridineethanamineHCID 83275—
ReactantHCID 13473186HCID 13473186—
ProductPhthalimideHCID 680993%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505911
Source datasetuspto-grants-1985_03
ORD IDord-891346c68e6f44fba9d4c1eeac3bac32
Source noteuspto-grants-1985_03