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HRID 245708作成日:2026年10月24日

Water → HCID 86674653、化合物

https://huagongshe.com/ja/reaction/245708

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Phosphorus oxychlorideHCID 24813—
反応物Sodium BicarbonateHCID 516892—
反応物N-((3-chloropyrazin-2-yl)methyl)-3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxamideHCID 86674652—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 86674653HCID 8667465325.1%

反応条件

温度60 °C

反応手順

To N-((3-chloropyrazin-2-yl)methyl)-3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxamide (1.382 mmol, 500 mg) in ethyl acetate (5 ml) at 0° C. was added phosphorus oxychloride (5.53 mmol, 0.515 ml). The reaction mixture was stirred at room temperature for two days and at 60° C. for one day. The reaction mixture was cooled to 0° C., an excess solid sodium hydrogencarbonate was added and the suspension was stirred at 0° C. for 10 minutes and at room temperature for 20 minutes. Then the suspension was again cooled to 0° C., water was added and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried (sodium sulfate) and concentrated in vacuo. The residue was purified by column chromatography (silica gel; dichloromethane applying a gradient 0 to 10% methanol) to give 7-(8-chloroimidazo[1,5-a]pyrazin-3-yl)-3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine (119 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658794B2
出典データセットuspto-grants-2014_02
ORD IDord-06c0737fdb9d4361bad3102fce058795
出典メモuspto-grants-2014_02