Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745835Generated: October 26, 2026

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

https://huagongshe.com/reaction/745835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminosulfonyl)-5-chlorophthalimideHCID 19733—
Reactant1-(4-Methoxybenzyl)piperidin-4-amineHCID 12641841—
Product1-PentanolHCID 6276—
Product6-Chloro-2,3-dihydro-2-[1-[(4-methoxyphenyl)methyl]-4-piperidinyl]-1,3-dioxo-1H-isoindole-5-sulfonamideHCID 23312449—

Reaction Steps

Reaction of 4-chloro-5-sulfamoylphthalimide (5.21 g., 0.02 mole) and 4-amino-1-(4-methoxybenzyl)piperidine (4.5 g., 0.02 mole) in 80 ml. of n-pentanol according to the procedure of Example 1(a) afforded the crude 1,3-dioxoisoindole product purified by chromatography (silica gel, ethyl acetate-n-hexane) to yield 2.88 g. (31%) of 6-chloro-2,3-dihydro-2-[1-[(4-methoxyphenyl)methyl]-4-piperidinyl]-1,3-dioxo-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-811d287b556843758a248cc3e7519b32
Source noteuspto-grants-1986_07