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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 566875Erstellt: 25. Oktober 2026

4-(Piperazin-1-yl)benzene-1-sulfonamide → 4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamide

https://huagongshe.com/reaction/566875

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Piperazin-1-yl)benzene-1-sulfonamideHCID 901897—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carbaldehydeHCID 10773638—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamideHCID 212639034,4%

Reaktionsschritte

Sodium triacetoxyborohydride (1.2 g, 5.9 mmol) is added to a solution of 3-oxo-3,4-dihydro-2H-benzo[1,4]-oxazine-6-carbaldehyde (0.5 g, 2.8 mmol) and 4-(piperazin-1-yl)-benzenesulfonamide (0.17 g, 3.1 mmol) in 20 mL of THF. The mixture is stirred at room temperature overnight. The reaction is quenched by addition of 50 mL of water, and the THF is removed under reduced pressure. The precipitate is collected by filtration and recrystallized from methanol to give 0.05 g (4% yield) of 4-[4-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethyl)-piperazin-1-yl]-benzenesulfonamide; mp 150-153° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06177422B1
Quelldatensatzuspto-grants-2001_01
ORD IDord-d0c80c34be8242cfb1bf393155c62d2b
Quellennotizuspto-grants-2001_01