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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542829생성일: 2026년 10월 25일

Piperazine → HCID 13077534, 화합물

https://huagongshe.com/reaction/542829

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물N-[6-Chlorohexyl]-6-methoxy-4-methyl-8-quinolinamineHCID 608631—
용매TolueneHCID 1140—
생성물HCID 13077534HCID 13077534—

반응 단계

A solution of 6.2 g (0.02 mole) of crude N-(6-chlorohexyl)-6-methoxy-4-methyl-8-quinolinamine in 75 ml of toluene was added dropwise to a stirred, hot suspension of 25 g (0.29 mole) of piperazine in 25 ml of toluene. The mixture was distilled until the internal temperature rose to 130°, allowed to cool, and taken up in a mixture of water and dichloromethane. The organic layer was separated, washed again, dried over anhydrous magnesium sulfate and concentrated to dryness in vacuo. The residual brown oil was chromatographed over 200 g of silica gel first with ethyl acetate and then with 500 ml each of the following solutions of methanol in ethyl acetate: 4%, 8%, 12% 16%, 20% and 25%. The eluant which appeared to contain only the product, Rf (silica--25 methanol:75 ethyl acetate:1 triethylamine)=0.05 was concentrated to dryness in vacuo. The residue was triturated with ether and filtered to remove 1 g of the bis product, mp 126°-128°, and concentrated again. The residue was dissolved in hot 2-propanol, filtered to remove haze and treated with a saturated solution of hydrogen chloride in 2-propanol. The resulting precipitate was collected, dried overnight at 60° in vacuo and allowed to air-equilibrate to afford 5.8 (60% ) of the title compound, mp 245°-247° (dec) with prior sintering at 125°. The NMR spectrum confirmed the presence of 2-propanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04659708
출처 데이터셋uspto-grants-1987_04
ORD IDord-5b1f06b667bd4e63946a8f6fdc571a00
출처 메모uspto-grants-1987_04