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HRID 520815作成日:2026年10月27日

Potassium Carbonate → 3-[2-(1-t-Butyloxycarbonyl piperidin-4-yloxy)pyridin-5-yl]-1-(morpholin-4-yl)prop-2-ene-1-one

https://huagongshe.com/reaction/520815

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物AcryloylmorpholineHCID 98723—
反応物tert-Butyl 4-((5-bromopyridin-2-yl)oxy)piperidine-1-carboxylateHCID 21914479—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物3-[2-(1-t-Butyloxycarbonyl piperidin-4-yloxy)pyridin-5-yl]-1-(morpholin-4-yl)prop-2-ene-1-oneHCID 9004272291.5%

反応手順

A solution of t-butyl 4-(5-bromo pyridin-2-yloxy)piperidine-1-carboxylate (1 gram, 2.80 mmoles), 4-acryloylmorpholine (0.63 gram, 4.46 mmoles), palladium acetate (13 mg, 0.061 mmoles) tri(o-tolyl)phosphine (25.6 mg, 0.084 mmoles) and potassium carbonate (0.62 g, 4.49 mmoles) in DMF (15 mL) was stirred for 3 hours at 140° C. The progress of the reaction was monitored by thin layer chromtography. After completion of reaction, the mass was quenched on to chilled water (30 mL) and the product was extracted with ethyl acetate (3×15 mL). The resulting organic layer was washed with water, dried over sodium sulfate and concentrated under vacuum. The residue, thus obtained, was purified by flash chromatography using ethyl acetate:n-hexane in the ratio of 1:1 to afford the title compound (1.07 grams).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328092B2
出典データセットuspto-grants-2016_05
ORD IDord-68b517314f804299a5a85ee2f2a0fa9c
出典メモuspto-grants-2016_05