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HRID 1493823作成日:2026年10月27日

Captopril → N-(1-Naphthyl)ethylenediamine

https://huagongshe.com/reaction/1493823

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 0.1 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05025001
出典データセットuspto-grants-1991_06
ORD IDord-eafd8c35ef524f519dd2535378776856
出典メモuspto-grants-1991_06