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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Cystamine Dihydrochloride | HCID 5941 | — |
| Edukt | Succinic anhydride | HCID 7922 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 4-Azidobenzene-1-sulfonyl chloride | HCID 548486 | — |
| Edukt | N-(p-azidobenzenesulfonyl)cystamine | HCID 19609016 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05646302 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-4b0c5cca47d5458eb1a85f5bdc314110 |
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| Quellennotiz | uspto-grants-1997_07 |
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