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HRID 52015作成日:2026年10月23日

Dimedone → 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2yl)oxy]-2-methylindol-4-carboxylic Acid

https://huagongshe.com/ja/reaction/52015

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 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2-yl)oxy]-2-methylindol-4-carboxylateHCID 19962751—
溶媒TetrahydrofuranHCID 8028—
生成物3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2yl)oxy]-2-methylindol-4-carboxylic AcidHCID 1996275493%

反応手順

0.49 g of allyl 3-acetylamino-5-[(4,6-dimethoxypyrimidin-2-yl)oxy]-2-methylindol-4-carboxylate was dissolved in 10 ml of tetrahydrofuran, and 0.1 g of dimedone and 0.01 g of tetrakistriphenylphosphine palladium were added thereto. The mixture was stirred at room temperature for 4 hours. Crystals obtained by concentration under reduced pressure, was washed with isopropyl ether to obtain 0.41 g (yield: 93%) of the desired compound. mp: 230°-233° C.

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-d8978749e11948fcb45208fd1bc39b1f
出典メモuspto-grants-1997_04