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HRID 83024作成日:2026年10月24日

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/ja/reaction/83024

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl acrylateHCID 15458—
反応物Tri-o-tolylphosphineHCID 80271—
反応物DiisopropylethylamineHCID 81531—
反応物6-Bromo-3-(2-(4-methylpiperazin-1-yl)ethyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-oneHCID 67154604—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
溶媒PropionitrileHCID 7854—
生成物(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—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846711B2
出典データセットuspto-grants-2014_09
ORD IDord-ded97ebc2630475bb9eed305cd572b04
出典メモuspto-grants-2014_09