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HRID 230374作成日:2026年10月24日

Ethyl Acetate → HCID 57762568、化合物

https://huagongshe.com/ja/reaction/230374

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物(S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762562—
反応物HCID 57762606HCID 57762606—
触媒Tri-o-tolylphosphineHCID 80271—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物HCID 57762568HCID 5776256863.3%

反応条件

温度80 °C

反応手順

Under an argon atmosphere, palladium acetate (19.9 mg) and tris(2-methylphenyl)phosphine (25.9 mg) were added to a suspension of (S)-2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (514.4 mg), N-(4-iodophenyl)-N-isopropylpyrimidin-2-amine (577.4 mg) and potassium carbonate (352.9 mg) in DMF (6 ml), and the resulting mixture was stirred at 80° C. for 7 hours. After cooling the reaction solution to room temperature, ethyl acetate was added thereto, and the resulting mixture was washed twice with water and once with saturated brine, followed by drying the organic layers over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform=2/1→1/1→1/3). The obtained crudely purified product was purified again by column chromatography (silica gel, eluent: cyclohexane/ethyl acetate=6/1-4/112/1) to obtain (S,E)-2-(2,6-dichlorobenzamido)-5-[4-(isopropyl-pyrimidin-2-ylamino)phenyl]pent-4-enoic acid methyl ester (553.6 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566724B2
出典データセットuspto-grants-2009_07
ORD IDord-1a0084c7803f4e85906fb173dba7cfc5
出典メモuspto-grants-2009_07