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HRID 54949作成日:2026年10月24日

Acetyl chloride → 3-(1-Acetyl-l,2-dihydro-2-methylpyridin-4-yl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/ja/reaction/54949

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物Sodium BicarbonateHCID 516892—
反応物2-(4-Fluorophenyl)-3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidineHCID 19957280—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物3-(1-Acetyl-l,2-dihydro-2-methylpyridin-4-yl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidineHCID 19957261—

反応手順

To a solution of 2-(4-fluorophenyl)-3-(pyridin-4-yl)pyrazolo[1,5-a]pyrimidine (480 mg) in dry tetrahydrofuran (15 ml) was added acetyl chloride (0.89 ml) dropwise under ice cooling. The mixture was stirred at ambient temperature for 1 hour and to the mixture was added a solution of methyl magnesium bromide in tetrahydrofuran (1 mole solution, 12.42 ml) under ice cooling. The mixture was stirred at ambient temperature for 2 hours and to the mixture was added an aqueous saturated sodium bicarbonate solution. The separated oil was extracted with dichloromethane and the solution was washed with brine, dried and concentrated in vacuo. The residue was purified by column chromatography on silica gel to give 3-(1-acetyl-1,2-dihydro-2-methylpyridin-4-yl)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyrimidine (327 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624931
出典データセットuspto-grants-1997_04
ORD IDord-433c0b0ad6fb44ebb147f39609782179
出典メモuspto-grants-1997_04