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HRID 20083作成日:2026年10月24日

Acetic Acid → Benzyl 4-{[1-(methoxycarbonyl)but-3-en-1-yl]amino}piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/20083

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Methyl 2-aminopent-4-enoateHCID 10877146—
溶媒1,1-DichloroethaneHCID 6365—
生成物Benzyl 4-{[1-(methoxycarbonyl)but-3-en-1-yl]amino}piperidine-1-carboxylateHCID 22293179103.4%

反応手順

Sodium triacetoxyborohydride (11.2 g, 52.6 mmol) was added to a solution of methyl 2-aminopent-4-enoate (3.4 g, 26.3 mmol), acetic acid (2.37 g, 39.5 mmol) and benzyl 4-oxopiperidine-1-carboxylate (9.21 g, 39.5 mmol) in dichloroethane (60 mL) at room temperature. After 3 h, the reaction was quenched with saturated aqueous sodium bicarbonate, extracted with methylene chloride (3×), dried over sodium sulfate, filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 0 to 8% methanol in methylene chloride gradient elution), which gave the title compound (9.42 g). MS 347.2 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745427B2
出典データセットuspto-grants-2010_06
ORD IDord-33c0580e28f64c06ae5e7467e5c2b669
出典メモuspto-grants-2010_06