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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244873생성일: 2026년 10월 26일

Methanol → 1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amine

https://huagongshe.com/reaction/244873

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2-ethyl-7-[2-(methylsulfonyl)ethenyl]-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 86629392—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 131731206—

반응 조건

온도50 °C

반응 단계

A glass Parr vessel was charged with 10% palladium on carbon (0.2 g), methanol (25 mL), ethanol (25 mL) and 2-ethyl-7-[2-(methylsulfonyl)ethenyl]-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amine (315 mg, 0.76 mmol). The vessel was evacuated and charged with hydrogen gas (40 psi, 2.8×105 Pa). The reaction was shaken at 50° C. for approximately 18 hours and then cooled to ambient temperature. The reaction mixture was sequentially filtered, concentrated under reduced pressure, and purified by chromatography using a HORIZON HPFC system (silica cartridge, eluting with CMA:chloroform gradient, 0-10% CMA over 1000 mL followed by 10-25% CMA over 1000 mL). A final recrystallization from acetonitrile provided 125 mg of 2-ethyl-7-[2-(methylsulfonyl)ethyl])-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-imidazo[4,5-c]quinolin-4-amine as a white crystalline solid, mp 246.5-249.0° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658666B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-bc16f9b6cb3b418c9e6439bacc98e01f
출처 메모uspto-grants-2014_02