HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Captopril → N-(1-Naphthyl)ethylenediamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Captopril | HCID 44093 | — |
| Edukt | S-Nitrosocaptopril | HCID 129596 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Lösungsmittel | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Produkt | N-(1-Naphthyl)ethylenediamine | HCID 15107 | — |
Reaktionsschritte
Typical preparation of S-nitrosocaptopril involve the reaction of 50 mM captopril with 50 mM NaNO2 in 0.1 N acetic or sulfuric acid at room temperature for five minutes, after which the reaction solution is passed over a cation exchange resin, e.g., Dowex 50 in the protonated form, and the product eluted with water. The fractions that give positive reactions with N-(1-naphthyl)ethylenediamine, after exposure to 0.15% HgCl2 and diazotization with sulfanilamide, are lyophilized. Hygroscopic, bright red crystals (m.p. 98-104° C.) were obtained that were shown to be S-nitrosocaptopril by NMR in deuterated DMSO and by mass spectroscopy.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05025001 |
| Quelldatensatz | uspto-grants-1991_06 |
| ORD ID | ord-eafd8c35ef524f519dd2535378776856 |
| Quellennotiz | uspto-grants-1991_06 |