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 preparations 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 were obtained that were
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05002964 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-855e4ea735f84408958842a4e014961c |
| Source note | uspto-grants-1991_03 |