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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83024생성일: 2026년 10월 25일

tert-Butyl acrylate → (E)-tert-Butyl 3-(3-(2-(4-methylpiperazin-1-yl)ethyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-6-yl)acrylate

https://huagongshe.com/reaction/83024

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl acrylateHCID 15458—
반응물Tri-o-tolylphosphineHCID 80271—
반응물DiisopropylethylamineHCID 81531—
반응물6-Bromo-3-(2-(4-methylpiperazin-1-yl)ethyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-oneHCID 67154604—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매PropionitrileHCID 7854—
생성물(E)-tert-Butyl 3-(3-(2-(4-methylpiperazin-1-yl)ethyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-6-yl)acrylateHCID 68338119—

반응 단계

tert-Butyl acrylate (830 μL, 5.64 mmol), diisopropylethylamine (500 □L, 2.82 mmol) and P(o-tolyl)3 (86 mg, 0.28 mmol) were successively added to a suspension of 6-bromo-3-(2-(4-methylpiperazin-1-yl)ethyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one (500 mg, 1.41 mmol) in propionitrile (6 mL) and dimethylformamide (2 mL). The resulting mixture was purged with argon prior to the addition of palladium acetate (32 mg, 0.14 mmol). The mixture was then purged a second time with argon and refluxed overnight. The reaction mixture was filtered on Celite® and washed with ethyl acetate (100 mL) and dichloromethane (100 mL). The filtrate was concentrated to dryness and the residue was solubilized in dichloromethane (100 mL). The resulting solution was washed with a saturated solution of sodium chloride (3×100 mL), dried over sodium sulfate, filtered and concentrated to dryness. The residue was purified by chromatography on silica gel using dichloromethane/methanol/ammoniac (1:0:0.1 to 98:2:0.1) as eluent. The title product was obtained as a brown solid (83 mg, 15%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846711B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ded97ebc2630475bb9eed305cd572b04
출처 메모uspto-grants-2014_09