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HRID 2039580作成日:2026年10月27日

Triphenylphosphine → methyl (E)-3-(2-{3-[6-oxo-3-(3,4,5-trifluorophenyl)-6H-pyridazin-1-ylmethyl]phenyl}pyrimidin-5-yl)acrylate

https://huagongshe.com/reaction/2039580

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物methyl (E)-3-[2-(3-hydroxymethylphenyl)pyrimidin-5-yl]acrylateHCID 58289762—
反応物6-(3,4,5-trifluorophenyl)-2H-pyridazin-3-oneHCID 59406809—
溶媒TetrahydrofuranHCID 8028—
生成物methyl (E)-3-(2-{3-[6-oxo-3-(3,4,5-trifluorophenyl)-6H-pyridazin-1-ylmethyl]phenyl}pyrimidin-5-yl)acrylateHCID 59484916—

反応手順

47.2 90 mg (0.4 mmol) of 6-(3,4,5-trifluorophenyl)-2H-pyridazin-3-one and 111 mg (0.41 mmol) of methyl (E)-3-[2-(3-hydroxymethylphenyl)-pyrimidin-5-yl]acrylate are suspended in 3 ml of THF with 200 mg (0.6 mmol) of polymer-bound triphenylphosphine (about 3 mmol of triphenylphosphine per g), and the mixture is shaken at room temperature for 30 min. The mixture is cooled to 0° C., and 95 μl (0.6 mmol) of diethyl azodicarboxylate are added. The reaction mixture is shaken at room temperature for 24 h. The reaction mixture is purified by means of preparative HPLC; yield: 7 mg of “A283”; HPLC: Rt=3.41 min (method C);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08580781B2
出典データセットuspto-grants-2013_11
ORD IDord-060fd3a423584c008ac274639ccf44e9
出典メモuspto-grants-2013_11