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HRID 751334생성일: 2026년 10월 25일

1-(2-Hydroxyethyl)piperazine → 2-[4-(2-hydroxyethyl)piperazin-1-yl]-1-phenyl-1H-indole-3-carboxaldehyde

https://huagongshe.com/reaction/751334

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Hydroxyethyl)piperazineHCID 7677—
반응물2-chloro-1-phenyl-1H-indole-3-carbaldehydeHCID 314793—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-[4-(2-hydroxyethyl)piperazin-1-yl]-1-phenyl-1H-indole-3-carboxaldehydeHCID 11175508—

반응 단계

2-Chloro-1-phenyl-1H-indole-3-carboxaldehyde (2.55 g, 19.6 mmol), 4-(2-hydroxyethyl)-piperazine (1.00 g, 3.92 mmol) in dioxane (13 mL) is heated overnight at reflux. The cooled reaction is diluted with water and extracted with dichloromethane. The organic layer is dried, filtered and evaporated to a semi-solid that is triturated with ether to give the 2-[4-(2-hydroxyethyl)piperazin-1-yl]-1-phenyl-1H-indole-3-carboxaldehyde as a brownish solid. MS 350 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07405300B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-bdbbc4a1fb4b43aeab0b598183467d36
출처 메모uspto-grants-2008_07