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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51270생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/51270

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참여 물질

역할이름HCID투입량
반응물VeratroleHCID 7043—
반응물4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl esterHCID 44203202—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanoneHCID 46780868—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713627B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-74e44df03d06443bac63a75ca0bbbe91
출처 메모uspto-grants-2004_03