戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 52007作成日:2026年10月23日

Dimedone → 5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylic Acid

https://huagongshe.com/ja/reaction/52007

反応式

関与物質

役割名称HCID仕込み量
反応物DimedoneHCID 31358—
反応物Allyl 5-(4,6-dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylateHCID 53832981—
溶媒TetrahydrofuranHCID 8028—
生成物5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylic AcidHCID 5446801991.4%

反応手順

1.60 g of allyl 5-(4,6-dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylate and 0.54 g of dimedone were dissolved in 14 ml of tetrahydrofuran, and 40 mg of tetrakistriphenylphosphine palladium (0) was added thereto under a nitrogen atmosphere. The mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to obtain 1.33 g (yield: 91%) of the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616537
出典データセットuspto-grants-1997_04
ORD IDord-20301908661145a2bcc9f8c17eecf4a7
出典メモuspto-grants-1997_04