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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745834Generated: October 26, 2026

1-Pentanol → 6-chloro-2,3-dihydro-2-[1-[(2-methylphenyl)methyl]-4-piperidinyl]-1,3-dioxo-1H-isoindole-5-sulfonamide

https://huagongshe.com/reaction/745834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentanolHCID 6276—
ReactantPhthalimideHCID 6809—
Reactant4-(Aminosulfonyl)-5-chlorophthalimideHCID 19733—
Reactant1-[(2-Methylphenyl)methyl]piperidin-4-amineHCID 12641834—
SolventHeptaneHCID 8900—
Product6-chloro-2,3-dihydro-2-[1-[(2-methylphenyl)methyl]-4-piperidinyl]-1,3-dioxo-1H-isoindole-5-sulfonamideHCID 13370607—

Reaction Steps

A mixture of 4-chloro-5-sulfamoylphthalimide (5.74 g., 0.022 mole) and 4-amino-1-[(2-methylphenyl)methyl]piperidine (4.5 g., 0.022 mole) in 85 ml. of n-pentanol was reacted according to the procedure of Example 1(a). Addition of n-heptane to the reaction mixture afforded 7.9 g. (80%) of the 1,3-dioxoisoindole product, m.p. 283°-243°. Crystallization of this material from DMF-methanol provided analytically pure 6-chloro-2,3-dihydro-2-[1-[(2-methylphenyl)methyl]-4-piperidinyl]-1,3-dioxo-1H-isoindole-5-sulfonamide, m.p. 244°-245° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04600758
Source datasetuspto-grants-1986_07
ORD IDord-aa54ee27ac754616ae29fd99a2216abc
Source noteuspto-grants-1986_07