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HRID 549405作成日:2026年10月24日

Methyl Acrylate → (E)-3-{4-[4-methyl-1-(2-pyrazolo[1,5-a]pyridin-3-yl-ethyl)-piperazin-2-yl]-phenyl}-acrylic acid methyl ester

https://huagongshe.com/ja/reaction/549405

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl AcrylateHCID 7294—
反応物N-Methyl dicyclohexylamineHCID 24210—
反応物3-{2-[2-(4-Bromo-phenyl)-4-methyl-piperazin-1-yl]-ethyl}-pyrazolo[1,5-a]pyridineHCID 57899247—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
触媒Tri-t-butylphosphine fluoroborateHCID 44558591—
溶媒1,4-DioxaneHCID 31275—
生成物(E)-3-{4-[4-methyl-1-(2-pyrazolo[1,5-a]pyridin-3-yl-ethyl)-piperazin-2-yl]-phenyl}-acrylic acid methyl esterHCID 5789930697.1%

反応条件

温度135 °C

反応手順

A mixture of 3-{2-[2-(4-bromo-phenyl)-4-methyl-piperazin-1-yl]-ethyl}-pyrazolo[1,5-a]pyridine (1.0 g, 2.49 mmol), methyl acrylate (0.458 mL, 4.98 mmol), N-methyldicyclohexylamine (584 mg, 2.99 mmol), tri-(tert-butyl)phosphine-tetrafluoroborate (28.9 mg, 0.0997 mmol) and Pd2(dba)3 (22.8 mg, 0.02 mmol) in 1,4-dioxane (10 mL) was flushed with nitrogen and heated at 100° C. for 1 h and at 135° C. for 1 h under microwave irradiation. The reaction mixture was cooled to room temperature, filtered through Celite pad, and concentrated in vacuo. Purification via flash silica gel column chromatography (heptane/ethyl acetate) gave (E)-3-{4-[4-methyl-1-(2-pyrazolo[1,5-a]pyridin-3-yl-ethyl)-piperazin-2-yl]-phenyl}-acrylic acid methyl ester (0.978 g, 97% yield). LCMS (m/z): 405.30 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943652B2
出典データセットuspto-grants-2011_05
ORD IDord-480eefb903c84f53899ee8b0122ec693
出典メモuspto-grants-2011_05