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HRID 2372880作成日:2026年10月26日

Beta-Alanine → N-carboxyethyl-amphetamine

https://huagongshe.com/reaction/2372880

反応式

関与物質

役割名称HCID仕込み量
反応物Beta-AlanineHCID 239—
反応物PhenylacetoneHCID 7678—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒MethanolHCID 887—
溶媒Ethyl AcetateHCID 8857—
生成物N-carboxyethyl-amphetamineHCID 1446324360.2%

反応手順

Phenylacetone (100 mg, 0.745 mmol) was dissolved in anhydrous methanol (2.0 ml). Beta-alanine (398 mg, 4.47 mmol) was added, followed by sodium cyanoborohydride (94 mg, 1.49 mmol). After 18 hours of stirring under nitrogen, the reaction mixture was filtered, and the filtrate solvent was removed in vacuo. The resulting crude material was purified on four 1.0 millimeter C18 reverse-phase preparative thin layer chromatography plates eluted with H2O/methanol/acetic acid (40/60/0.4). The material obtained was dissolved in ethyl acetate (20 ml) and was extracted with 1.0M sodium bicarbonate (3×20 ml). The aqueous extracts were combined, the pH was adjusted to 4 with 1.0M hydrochloric acid, and the solvent was removed in vacuo. The resulting crystalline solid was then triturated twice with 50-milliliter portions of ethyl acetate and filtered. The filtrates were combined, and the solvent was removed in vacuo to yield 93 milligrams of N-carboxyethyl-amphetamine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05101015
出典データセットuspto-grants-1992_03
ORD IDord-672d7e4cf34d4e9999d8f5472e7f45ad
出典メモuspto-grants-1992_03