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HRID 220084作成日:2026年10月26日

Ethanol → 5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine

https://huagongshe.com/reaction/220084

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Butanenitrile, 3-imino-HCID 70698—
反応物4-Hydrazinyl-6-(methylthio)pyrimidineHCID 13519855—
溶媒Ethyl AcetateHCID 8857—
生成物5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamineHCID 59173368—

反応条件

温度85 °C

反応手順

The mixture of (6-Methylsulfanyl-pyrimidin-4-yl)-hydrazine (1.0 g, 6.4 mmol), 3-Imino-butyronitrile (1.1 g, 12.8 mmol), and ethanol (30 mL) is heated to 85° C. for overnight. The reaction mixture is then cooled to room temperature, condensed, and treated with 75 mL ethyl acetate. The reaction mixture is partitioned between ethyl acetate and aqueous layer. The organic layer is dried over Na2SO4 and concentrated. The crude product is purified by ISCO chromatography eluting with ethyl acetate in hexanes from 10% to 80% to afford 5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine: 1H NMR 400 MHz (d6-DMSO) δ 8.72 (s, 1H), 7.53 (s, 1H), 6.90 (s, 1H), 5.26 (s, 1H), 2.57 (s, 3H), 2.08 (s, 3H); MS m/z 222.07 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08202876B2
出典データセットuspto-grants-2012_06
ORD IDord-e8f9c9326c874781be6fe58dad94815f
出典メモuspto-grants-2012_06