HuagongsheHuagongshe Chemistry Print Report · For research reference only
Captopril → N-(1-Naphthyl)ethylenediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Captopril | HCID 44093 | — |
| Reactant | S-Nitrosocaptopril | HCID 129596 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Product | N-(1-Naphthyl)ethylenediamine | HCID 15107 | — |
Reaction Steps
Typical preparation of S-nitrosocaptopril involve the reaction of 50 mM captopril with 50 mM NaNO2 in 0.1N 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05356890 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-dd03f2d1929c4906a123337dd8a492fe |
| Source note | uspto-grants-1994_10 |