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HRID 2253386作成日:2026年10月25日

Water → tert-Butyl N-[7-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-2-(methoxymethyl)pyrazolo[1,5-a]pyridin-3-yl)carbamate

https://huagongshe.com/reaction/2253386

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Barium hydroxide, octahydrateHCID 17749109—
反応物tert-butyl N-[7-bromo-2-(methoxymethyl)pyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 21084187—
反応物2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 23080945—
触媒HCID 178418397HCID 178418397—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物tert-Butyl N-[7-[2,6-dimethoxy-4-(methoxymethyl)phenyl]-2-(methoxymethyl)pyrazolo[1,5-a]pyridin-3-yl)carbamateHCID 2108418263.6%

反応条件

温度80 °C

反応手順

To a solution of tert-butyl N-[7-bromo-2-(methoxymethyl)pyrazolo[1,5-a]pyridin-3-yl]carbamate (300 mg) dissolved in 1,2-dimethoxyethane (10 mL) and water (5 mL) was added 2,6-dimethoxy-4-methoxymethylphenylboric acid (323 mg), tetrakis(triphenylphosphine)palladium(0) (146 mg) and barium hydroxide octahydrate (398 mg), and the reaction mixture was heated and stirred for 2 hours at 80° C. under a nitrogen stream. Water was added to the obtained reaction mixture, the reaction mixture was extracted with ethyl acetate, and the organic extract was washed with brine. The obtained organic extract was dried over anhydrous magnesium sulfate and filtered, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (245 mg) was obtained as a light yellow amorphous solid from the n-hexane:ethyl acetate (1:1) fraction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07323569B2
出典データセットuspto-grants-2008_01
ORD IDord-3d56129d2b65433987a215b88547beee
出典メモuspto-grants-2008_01