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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 745831Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/745831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-PentanolHCID 6276—
EduktPhthalimideHCID 6809—
Edukt4-(Aminosulfonyl)-5-chlorophthalimideHCID 19733—
Edukt1-((4-Chlorophenyl)methyl)piperidin-4-amineHCID 7130833—
Produkt6-chloro-2-[1-[(4-chlorophenyl)methyl]-4-piperidinyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamideHCID 13370602—

Reaktionsschritte

Reaction of 4-chloro-5-sulfamoylphthalimide (5.57 g., 0.0214 mole) and 4-amino-1-(4-chlorobenzyl)piperidine (4.8 g., 0.0214 mole) in 85 ml. of n-pentanol according to the procedure of Example 1(a) with heating at 130°-138° for a 48 hr. period afforded 7.07 g. (71%) m.p. 248°-250° (dec.) of the 1,3-dioxoisoindole product. A sample crystallized from dimethylformamide-methanol provided analytically pure 6-chloro-2-[1-[(4-chlorophenyl)methyl]-4-piperidinyl]-2,3-dihydro-1,3-dioxo-1H-isoindole-5-sulfonamide, m.p. 250°-251° (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04600758
Quelldatensatzuspto-grants-1986_07
ORD IDord-691cd2b016f94d458983ed72bf182b8c
Quellennotizuspto-grants-1986_07