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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 586380생성일: 2026년 10월 25일

Diisopropylethylamine → 1-[1-(4-Chloro-phenyl)-cyclobutanecarbonyl]-piperidin-3-ylmethyl alcohol

https://huagongshe.com/reaction/586380

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Piperidin-3-ylmethanolHCID 107308—
반응물1-(p-Chlorophenyl)cyclobutanecarboxylic acidHCID 602761—
반응물PyBroPHCID 2733179—
용매DichloromethaneHCID 6344—
생성물1-[1-(4-Chloro-phenyl)-cyclobutanecarbonyl]-piperidin-3-ylmethyl alcoholHCID 2190203543.4%

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온도0 °C

반응 단계

To a solution of 3-piperidinemethanol (5.0 g, 43.4 mmol), 1-(4-chlorophenyl)-1-cyclobutanecarboxylic acid (9.14 g, 43.4 mmol), and diisopropylethylamine (11.22 g, 86.8 mmol) in dichloromethane (100 mL) at 0° C. was added PyBroP® (22.26 g, 47.8 mmol). The reaction was stirred at 0° C. for 1 h and then at room temperature for 4 h. The reaction mixture was washed successively with water, 1 N HCl, water, sat. sodium bicarbonate solution, and water (100 mL each). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated by rotary evaporation. The residue was purified by chromatography on silica gel, eluting with dichloromethane/methanol (96:4) to give 5.8 g of the amide 1 as a thick gum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06936614B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-0a89286097084166ad907101fbf5a093
출처 메모uspto-grants-2005_08