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HRID 408498作成日:2026年10月26日

2-Methoxybenzaldehyde → 2-tert-Butoxycarbonylamino-5-[hydroxy-(2-methoxy-phenyl)-methyl]-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/408498

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethoxybenzaldehydeHCID 8658—
反応物Ethyl 2-((tert-butoxycarbonyl)amino)-1,3-thiazole-4-carboxylateHCID 22280595—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-tert-Butoxycarbonylamino-5-[hydroxy-(2-methoxy-phenyl)-methyl]-thiazole-4-carboxylic acid ethyl esterHCID 5860989748.3%

反応手順

Butyl lithium (2.5 M, 53 mL, 132 mmol) was slowly added to a solution of 2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid ethyl ester (16.4 g, 60 mmol) in anhydrous tetrahydrofuran (250 mL) at −78° C. under a nitrogen atmosphere. A solution of 2-methoxybenzaldehyde (10.89 g, 79.99 mmol) in tetrahydrofuran (50 mL) was then added dropwise at −78° C. The mixture was warmed slowly to room temperature and stirred for 15 hours. The reaction mixture was quenched with a saturated aqueous solution of ammonium chloride (500 mL). The separated aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and evaporated to dryness. The crude product was then purified by column chromatography to yield the pure product (12 g, 29 mmol, 48%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759335B2
出典データセットuspto-grants-2014_06
ORD IDord-751f3845f70c4c01b100c125cac34ad4
出典メモuspto-grants-2014_06