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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 641887생성일: 2026년 10월 25일

p-Toluenesulfonic acid → tert-butyl 4-(1-acetyl-1H-indol-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/641887

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물1-Acetyl-1H-indol-3-yl acetateHCID 583602—
용매TolueneHCID 1140—
생성물tert-butyl 4-(1-acetyl-1H-indol-3-yl)piperazine-1-carboxylateHCID 59259291—

반응 조건

온도120 °C

반응 단계

Into a 150 mL sealed tube was placed a solution of 1-acetyl-1H-indol-3-yl acetate (2.5 g, 11.51 mmol) in toluene (80 mL). To this was added tert-butyl piperazine-1-carboxylate (10.71 g, 57.55 mmol). To the mixture was added p-toluenesulfonic acid (400 mg, 2.33 mmol). The resulting solution was allowed to react, with stirring, overnight while the temperature was maintained at 120° C. in a bath of oil. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:1). The mixture was concentrated by evaporation under vacuum using a rotary evaporator. The resulting solution was diluted with 200 mL of ethyl acetate. The resulting mixture was washed 3 times with 200 mL of NaCl(aq.). The mixture was dried over Na2SO4. The residue was purified by eluting through a column with a 10:1 petroleum ether/ethyl acetate solvent system. This resulted in 2.9 g (72%) of tert-butyl 4-(1-acetyl-1H-indol-3-yl)piperazine-1-carboxylate as a purple solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696229B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-aac31a08a2a542ecaefc79b1615cad5f
출처 메모uspto-grants-2010_04