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HRID 222813作成日:2026年10月23日

Levodopa → Melevodopa

https://huagongshe.com/ja/reaction/222813

反応式

関与物質

役割名称HCID仕込み量
反応物LevodopaHCID 6047—
反応物Acetyl chlorideHCID 6367—
溶媒MethanolHCID 887—
生成物MelevodopaHCID 23497117.3%

反応条件

温度15 °C

反応手順

A 3-Liter three-necked round-bottom flask equipped with a cooling bath, a thermometer and a condenser was charged with 1.5 Liters methanol, and acetyl chloride (119 ml, 1.2 mol) was carefully added thereto at 0° C. The cooling bath was replaced with a heating mantle and the mixture was heated to 15° C. 60 grams (0.3 mol) of L-3-(3,4-dihydroxy-phenyl)alanine was then added and the reaction mixture was refluxed for 3 hours and thereafter concentrated under reduced pressure at 60° C. to afford 74.3 grams (100% yield) of Compound 2 (see, Scheme 1). The product structure was confirmed by 1H-NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207369B2
出典データセットuspto-grants-2012_06
ORD IDord-4a47b9208e444a0f9d11a7aa6fff6a61
出典メモuspto-grants-2012_06