戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 400504作成日:2026年10月25日

2-Fluoroaniline → N-(2-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/400504

反応式

関与物質

役割名称HCID仕込み量
反応物2-FluoroanilineHCID 9584—
反応物Benzoyl chloride, 3-(chlorosulfonyl)-HCID 77671—
反応物(6S)-1,4-Diazabicyclo(4.3.0)nonaneHCID 781249—
溶媒DichloromethaneHCID 6344—
生成物N-(2-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 46851310—

反応手順

To 3-(chlorosulfonyl)benzoyl chloride (0.521 g, 2.18 mmol) in anhydrous dichloromethane (10 mL) was added (S)-octahydropyrrolo[1,2-a]pyrazine (0.250 g, 1.98 mmol) in dichloromethane (4 mL) slowly over 10 minutes at room temperature. The mixture was stirred at room temperature for 5 hours. Then 2-fluoroaniline (1.54 g, 13.87 mmol) was added. The mixture was stirred at room temperature overnight and then concentrated. The residue was purified by chromatography on silica gel (dichloromethane, then methanol/dichloromethane=1:10) to give the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08741899B2
出典データセットuspto-grants-2014_06
ORD IDord-d942abd221534db3bb1ed208b2cab874
出典メモuspto-grants-2014_06