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HRID 411263作成日:2026年10月26日

Acetamidomalonic acid diethyl ester → Diethyl acetamido[(pyridin-3-yl)methyl]propanedioate

https://huagongshe.com/reaction/411263

反応式

関与物質

役割名称HCID仕込み量
反応物Acetamidomalonic acid diethyl esterHCID 14041—
反応物3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物Diethyl acetamido[(pyridin-3-yl)methyl]propanedioateHCID 1381791430.2%

反応手順

Sodium metal (1.40 g, 61 mmol) was dissolved in EtOH (100 mL) containing diethyl acetamidomalonate (6.62 g, 30.5 mmol) and 3-picolyl chloride hydrochloride (5.00 g, 30.5 mmol) were added. The mixture was heated to reflux for 6 hr, and then cooled and filtered to remove NaCl (washed with EtOH). The solvent was removed in vacuo and the mixture was taken up into saturated aqueous NaHCO3 (100 mL) and extracted with EtOAc (3×100 mL). The solvent was removed and the residue purified by silica gel flash chromatography (95:5 CH2Cl2/MeOH) to give diethyl 2-(3-pyridylmethyl)-2-acetamidomalonate (2.84 g, 30%). Diethyl 2-(3-pyridylmethyl)-2-acetamidomalonate was dissolved in 6N HCl (30 mL) and heated to reflux for 19 hr whereupon it was cooled to room temperature and the HCl solution was removed by evaporation in vacuo. The intermediate amino acid dihydrochloride salt was taken up into MeOH (30 mL) saturated with HCl gas and stirred for 3.5 hr. The MeOH/HCl was removed by evaporation in vacuo to give β-(3-pyridyl)alanine methyl ester dihydrochloride (2.235 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559127B1
出典データセットuspto-grants-2003_05
ORD IDord-5f7184d6a88e49faa76974ff0fc92f84
出典メモuspto-grants-2003_05