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HRID 17827作成日:2026年10月24日

Ethyl 3-(2-fluorophenyl)-3-oxopropanoate → HCID 178515544、化合物

https://huagongshe.com/ja/reaction/17827

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 3-(2-fluorophenyl)-3-oxopropanoateHCID 296342—
反応物HCID 178507266HCID 178507266—
溶媒Acetic AcidHCID 176—
生成物HCID 178515544HCID 178515544—

反応手順

5-Cyclopropyl-2H-pyrazol-3-ylamine (2.9 g, 0.0235 mol) was suspended in AcOH (18 ml), 3-(2-fluorophenyl)-3-oxopropionic acid ethyl ester (4.67 ml, 1.1 eq) was added and the mixture heated at reflux for 3 h. The mixture was cooled to rt and concentrated underreduced pressure. The residue was stirred with EtOAc and the solid collected by filtration to give 2 g of 2-cyclopropyl-5-(2-fluorophenyl)-4H-pyrazolo[1,5-a]pyrimidin-7-one. Step B: The compound from step A (1 g, 0.00371 mol) was dissolved in POCl3 (12 ml) and cooled to 0° C. N,N-dimethylaniline (1.4 ml, 3 eq) was added and the mixture heated at 80° C. for 16 h. The mixture was cooled to rt and the volatiles removed. The resulting residue was dissolved in CH2Cl2, poured onto ice, and taken to pH 8 with NaHCO3 (s). The CH2Cl2 layer was removed, washed with water, dried (MgSO4), and concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, hexane-EtOAc/hexane 1:9) to give 0.85 g of the title compound. LCMS: MH+=288.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741318B2
出典データセットuspto-grants-2010_06
ORD IDord-bfbb1a8bfbbb4d4f994bce1798bea719
出典メモuspto-grants-2010_06