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HRID 51270作成日:2026年10月26日

Veratrole → N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone

https://huagongshe.com/reaction/51270

反応式

関与物質

役割名称HCID仕込み量
反応物VeratroleHCID 7043—
反応物4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl esterHCID 44203202—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanoneHCID 46780868—

反応条件

温度0 °C

反応手順

A solution of n-BuLi (2.5M, 452 mL) in hexane was added to a solution of veratrole (149 g, 1.08 mol) in anhydrous tetrahydrofuran (1.2 L) over 10 minutes at −78° C. under nitrogen. The resulting solution was stirred at 0° C. for 1 hour and room temperature for 4 hours. A solution of 4-[(methoxymethylamino)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (15) (275 g, 1.01 mol) in tetrahydrofuran (800 mL) was added to the reaction slurry at −65° C. over 20 minutes. The mixture was warmed to room temperature, stirred for 18 hours and quenched with saturated ammonium chloride (1 L). After stirring for 1 hour, the phases were separated and the aqueous layer was extracted with ethyl ether (1 L). The combined organic solutions were washed with brine (2 L) and dried (MgSO4). The mixture was filtered and the filtrate was concentrated (30° C./20 torr) to a residue (413 g). The solution may be used directly in Scheme L, step a, Example 108.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713627B2
出典データセットuspto-grants-2004_03
ORD IDord-74e44df03d06443bac63a75ca0bbbe91
出典メモuspto-grants-2004_03