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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745838Generated: November 3, 2026

4-(Aminosulfonyl)-5-chlorophthalimide → 1-Pentanol

https://huagongshe.com/reaction/745838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminosulfonyl)-5-chlorophthalimideHCID 19733—
Reactant1-{[3-(Trifluoromethyl)phenyl]methyl}piperidin-4-amineHCID 12888929—
Product1-PentanolHCID 6276—
Product6-Chloro-2,3-dihydro-1,3-dioxo-2-[1-[[3-(trifluoromethyl)-phenyl]methyl]-4-piperidinyl]-1H-isoindole-5-sulfonamideHCID 23312441—

Reaction Steps

Reaction of 4-chloro-5-sulfamoylphthalimide (10.1 g., 0.0386 mole) and 4-amino-1-(3-trifluoromethylbenzyl)piperidine (10.0 g., 0.0386 mole) in 200 ml. of n-pentanol according to the procedure of Example 1(a) afforded the crude 1,3-dioxoisoindole product purified by chromatography to yield 8.1 g. (42% yield) of 6-chloro-2,3-dihydro-1,3-dioxo-2-[1-[[3-(trifluoromethyl)phenyl]methyl]-4-piperidinyl]-1H-isoindole-5-sulfonamide. The NMR spectral data was consistent for the compound used without further purification below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04600758
Source datasetuspto-grants-1986_07
ORD IDord-e74e18e5ef02406a8c173ea654bdb8ef
Source noteuspto-grants-1986_07