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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583602생성일: 2026년 10월 25일

Piperazine → N-benzyl-5-(1-piperazinyl)indole

https://huagongshe.com/reaction/583602

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물1-Benzyl-5-Bromo-1H-IndoleHCID 285756—
용매O-XyleneHCID 7237—
생성물N-benzyl-5-(1-piperazinyl)indoleHCID 2209654689%

반응 조건

온도110 °C

반응 단계

A flask was charged with 75 ml of o-xylene, 6.21 g of N-benzyl-5-bromoindole, 11.2 g of piperazine and 2.85 g of NaOBut. The flask was flushed with nitrogen for 10 minutes, and then, 6.0 mg of palladium acetate (the ratio of palladium atom/N-benzyl-5-bromoindole=0.10% by mole) and 0.07 ml of a solution in toluene of tri-tert.-butylphosphine having a concentration of 0.25 g/ml were added into the flask. Then the content was heated to 110° C. and maintained at that temperature for 3 hours. Extraction, drying and concentration were conducted, and finally recrystallization was conducted from toluene to give N-benzyl-5-(1-piperazinyl)indole. The yield was 89% by mole on the basis of N-benzyl-5-bromoindole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929281
출처 데이터셋uspto-grants-1999_07
ORD IDord-21ba00057ca044018dbf82745cd2af83
출처 메모uspto-grants-1999_07