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HRID 1707947作成日:2026年10月27日

Captopril → N-(1-Naphthyl)ethylenediamine

https://huagongshe.com/reaction/1707947

反応式

関与物質

役割名称HCID仕込み量
反応物CaptoprilHCID 44093—
反応物S-NitrosocaptoprilHCID 129596—
反応物Sodium NitriteHCID 23668193—
溶媒Sulfuric AcidHCID 1118—
溶媒Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
生成物N-(1-Naphthyl)ethylenediamineHCID 15107—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05356890
出典データセットuspto-grants-1994_10
ORD IDord-dd03f2d1929c4906a123337dd8a492fe
出典メモuspto-grants-1994_10