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HRID 490116作成日:2026年10月26日

Acetic Acid → 6-Methyl-3-(6-(methylsulfinyl)pyrimidin-4-yl)pyrazolo[1,5-a]pyrimidin-2-amine

https://huagongshe.com/reaction/490116

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物m-Chloroperbenzoic acidHCID 70297—
反応物3-Ethoxy-2-methyl-2-propenalHCID 559198—
反応物4-(6-(methylthio)pyrimidin-4-yl)-1H-pyrazole-3,5-diamineHCID 57674529—
溶媒IsopropanolHCID 3776—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium HydroxideHCID 14798—
生成物6-Methyl-3-(6-(methylsulfinyl)pyrimidin-4-yl)pyrazolo[1,5-a]pyrimidin-2-amineHCID 5767459530%

反応条件

温度160 °C

反応手順

4-(6-(methylthio)pyrimidin-4-yl)-1H-pyrazole-3,5-diamine (1.0 g, 4.5 mmol) was combined with 3-ethoxy-2-methylacrylaldehyde (0.63 g, 5.3 mmol) in isopropanol (12 mL). Acetic acid (0.1 mL) was added to the reaction mixture which was then sealed in a microwave vessel and heated to 160° C. for 15 min. The reaction mixture was diluted with ethyl acetate (200 mL) and 1N NaOH (60 mL), the layers separated and the organic layer concentrated to 60 mL. This solution was cooled to 0° C. and 77% m-chloroperbenzoic acid (1.9 g, 8.5 mmol) was added. After 1 hr. a yellow precipitate formed which was filter off, washed with ethyl acetate and dried to give the product, 0.39 g, 30% yield. LCMS MH+289.29. H NMR (500 MHz, DMSO-d6) 9.02 (s, 1H) 8.91 (s, 1H), 8.88 (s, 1H), 8.54 (s, 1H), 7.14 (s, 2H), 2.91 (s, 3H), 2.34 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528138B2
出典データセットuspto-grants-2009_05
ORD IDord-5c8de0bb817b4576a1026089a29adc09
出典メモuspto-grants-2009_05