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HRID 633978作成日:2026年10月26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/reaction/633978

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US09321769B2
出典データセットuspto-grants-2016_04
ORD IDord-0b49e5c86efd403d9dbb80ea1e8e81d8
出典メモuspto-grants-2016_04