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HRID 1386872作成日:2026年10月27日

Hydrochloric Acid → N-(3,4-dihydroxyphenethyl)-2-(3,4-dihydroxyphenyl)-2-hydroxyacetamide

https://huagongshe.com/reaction/1386872

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Dopamine HydrochlorideHCID 65340—
反応物N-HydroxysuccinimideHCID 80170—
反応物(+-)-3,4-Dihydroxymandelic acidHCID 85782—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物N-(3,4-dihydroxyphenethyl)-2-(3,4-dihydroxyphenyl)-2-hydroxyacetamideHCID 9797093—

反応手順

2-(3,4-Dihydroxyphenyl)-2-hydroxyacetic acid (300 mg, 1.63 mmol) and N-hydroxysuccinimide (188 mg, 1.63 mmol) were dissolved in 1,4-dioxane (20 ml) under nitrogen, and N,N′-dicyclohexylcarbodiimide (336 mg, 1.63 mmol) was added to the mixture at room temperature, which was stirred at this temperature for 16 h. The by-product which precipitated out was filtered off, and the filtrate was added to a solution of 2-(3,4-dihydroxyphenyl)ethylamine hydrochloride (309 mg, 1.63 mmol) in water (20 ml). Sodium hydrogencarbonate (151 mg, 1.8 mmol) was also added, and the reaction mixture was stirred under nitrogen at 50° C. for 1.5 h. The mixture was rendered acidic using 5% strength hydrochloric acid and extracted 3 times with ethyl acetate (a total of 90 ml). The organic phase was washed with saturated NaCl solution, dried over Na2SO4 and filtered, and the filtrate was evaporated under reduced pressure. The product was purified by chromatography on silica gel using the eluent ethyl acetate. The yield was 266 mg of a colorless syrup (51% of theory based on the acid used).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06265611B1
出典データセットuspto-grants-2001_07
ORD IDord-752eb719072e47dc8f7bd6dcb8c146fd
出典メモuspto-grants-2001_07