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HRID 542829作成日:2026年10月25日

Piperazine → HCID 13077534、化合物

https://huagongshe.com/reaction/542829

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物N-[6-Chlorohexyl]-6-methoxy-4-methyl-8-quinolinamineHCID 608631—
溶媒TolueneHCID 1140—
生成物HCID 13077534HCID 13077534—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04659708
出典データセットuspto-grants-1987_04
ORD IDord-5b1f06b667bd4e63946a8f6fdc571a00
出典メモuspto-grants-1987_04