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HRID 57082作成日:2026年10月26日

Tetrahydrofuran → methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/57082

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Ceric ammonium nitrateHCID 180504—
反応物Methyl 3-chloro-1-(pyridine-3-yl)-4,5-dihydro-1H-pyrazole-5-carboxylateHCID 118022669—
溶媒WaterHCID 962—
生成物methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434712B2
出典データセットuspto-grants-2016_09
ORD IDord-b97d2d1d8aee4941b85b5295b8212e23
出典メモuspto-grants-2016_09