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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20975생성일: 2026년 10월 23일

Acetic Acid → 5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indole

https://huagongshe.com/ko/reaction/20975

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium CarbonateHCID 10340—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Indole-5-carboxaldehydeHCID 589040—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indoleHCID 6848993447%

반응 단계

5-Formylindole (500 mg, 3.44 mmol) was dissolved in acetonitrile (10 mL), and the solution was added with 1-(tert-butoxycarbonyl)piperazine (961 mg, 5.16 mmol), acetic acid (3.90 mL, 68.1 mmol) and sodium triacetoxyborohydride (3.65 g, 17.2 mmol) little by little, followed by stirring at room temperature for 2 hours. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography (hexane/ethyl acetate=19/1, 7/3, 1/1) to obtain 5-[4-(tert-butoxycarbonyl)piperazin-1-ylmethyl]indole (505 mg, yield 47%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-40825bde11ad4d73a783930ebca6be83
출처 메모uspto-grants-2010_06