関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate | HCID 21984654 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Ethylpyrazolo[1,5-a]pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091215B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-e2417cce65cb4c1590485a0406f53f9b |
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| 出典メモ | uspto-grants-2006_08 |
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