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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1668535생성일: 2026년 10월 26일

Tert-Butylamine → 5-(6-Hydroxymethylpyridin-2-yl)-1-(4-methylpiperazin-1-yl)pent-4-yn-1-one

https://huagongshe.com/reaction/1668535

반응식

참여 물질

역할이름HCID투입량
반응물Tert-ButylamineHCID 6385—
반응물(6-Bromopyridin-2-yl)methanolHCID 3517811—
반응물1-(4-Methylpiperazin-1-yl)pent-4-yn-1-oneHCID 57713812—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물5-(6-Hydroxymethylpyridin-2-yl)-1-(4-methylpiperazin-1-yl)pent-4-yn-1-oneHCID 5955542673%

반응 조건

온도80 °C

반응 단계

To a 50 mL round-bottom flask, 484 mg of 2-bromopyridine-6-methanol, 510 mg of 1-(4-methylpiperazin-1-yl)pent-4-yn-1-one, 20 mg of BHT, 162 mg of copper(I) iodide, 118 mg of tetrakis(triphenylphosphine)palladium (0), 375 mg of t-butylamine and 7.5 mL of DMF were added, and the mixture was stirred under argon atmosphere at 80° C. for 6 hours. The DMF was removed under reduced pressure, then saturated aqueous sodium bicarbonate was added thereto, and the mixture was extracted with chloroform. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was removed. The residue was purified by chromatography on silica gel (methylene chloride-methanol-triethylamine=600:20:1) to give 540 mg of 5-(6-hydroxymethylpyridin-2-yl)-1-(4-methylpiperazin-1-yl)pent-4-yn-1-one as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07989446B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-d2bdbbaf5ebd4324adf4133c98694e42
출처 메모uspto-grants-2011_08