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HRID 1366215作成日:2026年10月25日

4-Methoxybenzylamine → 5-Bromo-2-[(4-methoxy-benzylamino)-methyl]-furan-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/1366215

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxybenzylamineHCID 75452—
反応物Methyl 5-bromo-2-(bromomethyl)furan-3-carboxylateHCID 15534191—
溶媒MethanolHCID 887—
生成物5-Bromo-2-[(4-methoxy-benzylamino)-methyl]-furan-3-carboxylic acid methyl esterHCID 59023123—

反応手順

A solution of 5-bromo-2-bromomethyl-furan-3-carboxylic acid methyl ester (1.74, 5.88 mmol) and p-methoxy benzylamine (0.76 mL, 5.88 mmol) in MeOH (30 mL) is stirred at 85° C. for 1.5 hours. The reaction mixture is concentrated in vacuo and the residue purified by silica gel column chromatography eluting with 4:1 petroleum ether:ethyl acetate followed by 1:1 petroleum ether:ethylacetate. The title compound is isolated (643.8 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893058B2
出典データセットuspto-grants-2011_02
ORD IDord-e930bd0f854a463d8e3859144d92c6cc
出典メモuspto-grants-2011_02