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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264794Erstellt: 26. Oktober 2026

Hydrochloric Acid → N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine

https://huagongshe.com/reaction/264794

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktCystamine DihydrochlorideHCID 5941—
EduktSuccinic anhydrideHCID 7922—
EduktSodium HydroxideHCID 14798—
Edukt4-Azidobenzene-1-sulfonyl chlorideHCID 548486—
EduktN-(p-azidobenzenesulfonyl)cystamineHCID 19609016—
LösungsmittelWaterHCID 962—
ProduktN-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamineHCID 19609019—

Reaktionsschritte

2.2 g of cystamine dihydrochloride were dissolved in 20 ml of water and adjusted to pH 10 with NaOH. 2.1 g of p-azidobenzenesulfonyl chloride were suspended in this solution and the suspension was stirred at room temperature for 5 hours. The precipitated N-(p-azidobenzenesulfonyl)cystamine was reacted with 2 g of succinic anhydride and stirred overnight. The resulting solution was acidified with HCl, subsequently filtered and washed with water. The residue was dried at room temperature in a high vacuum and gave 1.53 g of N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine. The IR showed bands at 3283 (amide NH) 2134 (azide), 1714 (acid carbonyl), 1650 (amide), 1589+1547 (aromatic), 1284 (COOH), 1328+1180 (arylsulfonyl ), 839 (p-disubst.benzene). TLC (silica gel--NH3 conc./EtOH=1%) Rf=0.7. m.p.: dec. at 163°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646302
Quelldatensatzuspto-grants-1997_07
ORD IDord-4b0c5cca47d5458eb1a85f5bdc314110
Quellennotizuspto-grants-1997_07