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HRID 28765作成日:2026年10月25日

Gabapentin → Boc-Asp(OMe) Gabapentin

https://huagongshe.com/reaction/28765

反応式

関与物質

役割名称HCID仕込み量
反応物GabapentinHCID 3446—
反応物N-HydroxysuccinimideHCID 80170—
反応物Sodium BicarbonateHCID 516892—
反応物(2S)-2-{[(tert-butoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acidHCID 10977771—
溶媒AcetonitrileHCID 6342—
生成物Boc-Asp(OMe) GabapentinHCID 13172701398%

反応手順

To a solution of Boc-Asp(OMe)-OH (5 g, 20 mmol) in acetonitrile (100 mL) was added N-hydroxysuccinimide (2.53 g, 22 mmol) and N,N-dicyclohexylcarbodiimide (4.5 g, 22 mmol). The reaction was stirred at ambient temperature for 4 h. The reaction mixture was filtered directly into an aqueous solution (100 mL) of gabapentin (3.77 g, 22 mmol) and sodium hydrogencarbonate (1.85 g, 22 mmol) and the resulting mixture stirred at ambient temperature for 16 h. The reaction was concentrated under reduced pressure, the residue dissolved in ethyl acetate/diethyl ether (1:1, 300 mL) and washed with 0.1M aqueous potassium hydrogensulfate (2×500 mL). The organic phase was separated, dried over Na2SO4, filtered, and concentrated to dryness under reduced pressure to afford Boc-Asp(OMe)-Gabapentin as a white solid (7.8 g, 19.5 mmol, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420002B2
出典データセットuspto-grants-2008_09
ORD IDord-a5352857d5b9435d9c482e161179277d
出典メモuspto-grants-2008_09