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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227308생성일: 2026년 10월 25일

Ethylene Glycol → 4-[4-(t-Butoxycarbonyl)piperazin-1-yl]-3-(1-naphthylthio)-1H-indazole

https://huagongshe.com/reaction/227308

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Potassium CarbonateHCID 11430—
반응물1-NaphthalenethiolHCID 68259—
반응물HCID 178452228HCID 178452228—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매IsopropanolHCID 3776—
용매Ethyl AcetateHCID 8857—
생성물4-[4-(t-Butoxycarbonyl)piperazin-1-yl]-3-(1-naphthylthio)-1H-indazoleHCID 5890478345%

반응 단계

A mixture of 4-[4-(t-butoxycarbonyl)piperazin-1-yl]-3-iodo-1H-indazole (0.068 g, 0.159 mmol), copper(I) iodide (0.005 g, 0.024 mmol) and potassium carbonate (0.044 g, 0.318 mmol) are added to a screw-capped test tube with a Teflon-lined septum. The tube is evacuated and backfilled with argon and this procedure repeated twice more. The reaction mixture is treated sequentially with 2-propanol (1.5 mL), ethylene glycol (19 μL, 0.318 mmol) and 1-naphthalenethiol (0.051 g, 0.318 mmol), heated at 130°-140° C. for 8 h, cooled to room temperature, diluted with ethyl acetate and filtered through diatomaceous earth. The filtrate is concentrated under reduced pressure. The resultant crude material is purified by flash chromatography (silica gel, 40:60 ethyl acetate/hexanes) to afford the title compound as a colorless oil, 0.033 g (45% yield), identified by NMR and mass spectral analyses.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560470B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-306fa838894a4c9a85c2abf0057dcb50
출처 메모uspto-grants-2009_07