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Tetrahydrofuran → methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Ceric ammonium nitrate | HCID 180504 | — |
| 反応物 | Methyl 3-chloro-1-(pyridine-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate | HCID 118022669 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate | HCID 118022666 | — |
反応手順
In step b of Scheme 2, methyl 3-chloro-1-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylate (6c) is oxidized with diammonium cerium (IV) nitrate (CAN) in water and polar solvents such as tetrahydrofuran at temperatures from about 0° C. to about 30° C. to yield methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate (6d). It was surprisingly discovered that the oxidation in step b can also proceed with potassium permanganate (KMnO4) as the oxidant in polar solvents such as acetone at temperatures from about 0° C. to about 30° C. However, many standard oxidation procedures such as, for example potassium persulfate (K2S2O8), iodine pentoxide (I2O5), copper oxide (CuO), and hydrogen peroxide were found to be inoperative.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434712B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-b97d2d1d8aee4941b85b5295b8212e23 |
| 出典メモ | uspto-grants-2016_09 |