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HRID 9180作成日:2026年10月25日

N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate → 2-Ethylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/9180

反応式

関与物質

役割名称HCID仕込み量
反応物N-amino-2-(1-butynyl)pyridinium mesitylenesulfonateHCID 21984654—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物2-Ethylpyrazolo[1,5-a]pyridineHCID 16116261—

反応手順

A 6.1 g portion of the obtained N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate was dissolved in tetrahydrofuran (600 mL), potassium tert-butoxide (3.55 g) was added at room temperature, and the mixture was vigorously stirred for 30 minutes. After adding ice water to the reaction mixture, extraction was performed with ethyl acetate. The aqueous layer was again extracted with ethyl acetate, the insoluble portion was filtered with a celite filter, and the organic layers were combined and washed with brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (0.63 g) was obtained from the n-hexane:ethyl acetate (10:1) fraction as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091215B2
出典データセットuspto-grants-2006_08
ORD IDord-e2417cce65cb4c1590485a0406f53f9b
出典メモuspto-grants-2006_08