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HRID 1595329作成日:2026年10月26日

4-Methoxynaphthalen-1-ylmethylamine → Ethyl 2-(4-methoxy-1-naphthyl)-5-(4-methylphenyl)-imidazole-4-carboxylate

https://huagongshe.com/reaction/1595329

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methoxynaphthalen-1-ylmethylamineHCID 59139—
反応物HCID 178472891HCID 178472891—
生成物Ethyl 2-(4-methoxy-1-naphthyl)-5-(4-methylphenyl)-imidazole-4-carboxylateHCID 17847021484.5%

反応手順

Ethyl 2-hydroxyimino-3-(4-methylphenyl)-3-oxopropionate (16.0 g) and 1-(aminomethyl)-4-methoxynaphthalene (15.3 g) were reacted and treated in the same manner as in Starting Material Synthetic Example 1 to give ethyl 2-(4-methoxy-1-naphthyl)-5-(4-methylphenyl)-imidazole-4-carboxylate (22.2 g), which was dissolved in ethyl alcohol (450 ml), and the mixture was reacted and treated in the same manner as in Starting Material Synthetic Example 2 to give 2-(4-methoxy-1-naphthyl)-5-(4-methylphenyl)imidazole-4-carboxylic acid (12.1 g), melting point 226° C. (decomposition).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06288061B1
出典データセットuspto-grants-2001_09
ORD IDord-8c715b29413d4628a9332231345b9669
出典メモuspto-grants-2001_09