戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 128901作成日:2026年10月25日

Diethylhydroxylamine → 2-[5-(N,N-diethylaminooxycarbonylmethylthio)-4-chloro-2-fluorophenyl]-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione

https://huagongshe.com/reaction/128901

反応式

関与物質

役割名称HCID仕込み量
反応物DiethylhydroxylamineHCID 19463—
反応物2-(5-carboxymethylthio-4-chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-2H-isoindole-1,3-dioneHCID 13454494—
溶媒TetrahydrofuranHCID 8028—
生成物2-[5-(N,N-diethylaminooxycarbonylmethylthio)-4-chloro-2-fluorophenyl]-4,5,6,7-tetrahydro-2H-isoindole-1,3-dioneHCID 5716779872.5%

反応手順

In 20 ml of tetrahydrofuran, 1.85 g of 2-(5-carboxymethylthio-4-chloro -2-fluorophenyl)-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione was dissolved, to which 0.97 g of N,N'-carbonyldiimidazole was added and the resultant mixture was stirred for 30 minutes at room temperature. To the resultant mixture, 0.53 g of N,N-diethylhydroxylamine was added, and the resultant mixture was stirred for 2 hours at room temperature. After completion of the reaction, the reaction mixture was poured into a saturated saline solution and extracted with ethyl acetate. The extract was washed with a saturated saline solution, dried with anhydrous magnesium sulfate, and evaporated to remove the solvent under reduced pressure. The residue was purified by silica gel chromatography (eluent; hexane:ethyl acetate=5:1 to 3:1), which afforded 1.60 g of 2-[5-(N,N-diethylaminooxycarbonylmethylthio)-4-chloro-2-fluorophenyl]-4,5,6,7-tetrahydro-2H-isoindole-1,3-dione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05466663
出典データセットuspto-grants-1995_11
ORD IDord-ef54eb675b9041be86bab5c4850f5a93
出典メモuspto-grants-1995_11