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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271528생성일: 2026년 10월 25일

N,N-Dimethylglycine → 5-{5-[1-(2-Dimethylamino-ethanoyl)-piperidin-4-yl]-2-pyridin-4-yl-furan-3-yl}-indan-1-one oxime

https://huagongshe.com/reaction/271528

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylglycineHCID 673—
반응물TriethylamineHCID 8471—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물5-(5-Piperidin-4-yl-2-pyridin-4-yl-furan-3-yl)-indan-1-oneHCID 69314608—
용매DimethylformamideHCID 6228—
생성물5-{5-[1-(2-Dimethylamino-ethanoyl)-piperidin-4-yl]-2-pyridin-4-yl-furan-3-yl}-indan-1-one oximeHCID 13635525347%

반응 단계

A mixture of the product from Example 31 Step 5 (0.17 g, 0.47 mmol), N-cyclohexylcarbodiimide,N′-methyl polystyrene resin (0.4 g, 0.65 mmol, 1.7 mmol/g), and 1-hydroxybenzotriazole hydrate (0.081 g, 0.6 mmol) were suspended in DMF (4 ml) and treated with triethylamine (0.084 ml, 0.6 mmol) and dimethylamino-acetic acid (0.048 g, 0.47 mmol). The reaction was stirred at room temperature for 16 hours and filtered on to a 10 g SCX cartridge (Varian Mega Bond Elute). The cartridge was then washed with methanol and then a 1:90.880 ammonia:methanol solution. The ammonia containing fractions were then reduced in vacuo and the residue purified by chromatography on silica gel eluting with a mixture of 0.880 ammonia/methanol/chloroform (0.5:4.5:95) to afford the title compound (0.097 g, 47%); MS (ES+) m/e 444 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452906B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-91602fe5b292464596a6dd3e26314c35
출처 메모uspto-grants-2008_11