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HRID 17871作成日:2026年10月24日

Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylate → Benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/ja/reaction/17871

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
反応物2-Benzyl-4-methoxy-N-methylbenzamideHCID 22555927—
反応物Isopropanol carbon dioxideHCID 86586944—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物Benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylateHCID 6843349049.4%

反応手順

To an isopropanol/dry ice cooled solution of 4-Methoxy-N-methyl-2-(phenylmethyl)benzamide (250 mg, 0.980 mmol) in THF (50 mL) under argon was added sec-butyllithium solution (1.3M, 1.55 mL, 2.00 mmol) dropwise. After 10 min. a THF (10 mL) solution of benzyl-4-(chlorocarbonyl)piperidine-1-carboxylate (275 mg, 980 mmol) was quickly added to the reaction solution. After 10 min. the reaction was quenched with water then warmed to room temperature. Saturated sodium bicarbonate was added and the resulting mixture extracted with ethyl acetate (3×) and dried with anhydrous magnesium sulfate. Filtration followed by evaporation of solvent in vacuo gave the crude product which was subjected to flash column chromatography (hexane:ethyl acetate 50:50) to afford benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate as a white foam (242 mg, 0.484 mmol, 49%). MS [M+H]+ 501.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741322B2
出典データセットuspto-grants-2010_06
ORD IDord-cdf90ed4d8804be8853d1f11965f5421
出典メモuspto-grants-2010_06