戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 877632作成日:2026年10月26日

3-(Morpholine-4-sulfonyl)benzohydrazide → N-[(E)-1-(5-chloro-2-fluorophenyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamide

https://huagongshe.com/reaction/877632

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Morpholine-4-sulfonyl)benzohydrazideHCID 877246—
反応物1-(5-Chloro-2-fluorophenyl)ethanoneHCID 2773579—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物N-[(E)-1-(5-chloro-2-fluorophenyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamideHCID 8658092019.22%

反応条件

温度120 °C

反応手順

1-(5-chloro-2-fluorophenyl)ethanone (20 mg, 0.116 mmol) and 3-(morpholinosulfonyl)benzohydrazide (33.1 mg, 0.116 mmol) was dissolved in Methanol (Volume: 4 ml) in the presence of acetic acid as a catalyst and then the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. Reaction was monitored by TLC. After completion of the reaction, following cooling, the solvent was removed by vacuum and the resulting crude material was purified by flash column chromatography (2% CH3OH/CH2Cl2) afforded the title compound (E)-N′-(1-(5-chloro-2-fluorophenyl)ethylidene)-3-(morpholinosulfonyl)benzohydrazide (10 mg, 0.022 mmol, 19.22% yield) as a solid. 1H NMR (CDCl3, 400 MHz): δ 8.26 (m, 1H), 8.09 (m, 1H), 7.80 (d, 1H, J=7.6 Hz), 7.58 (t, 1H, J=7.6 Hz), 7.37 (m, 1H), 7.21 (m, 1H), 6.95 (m, 1H), 3.61 (m, 4H), 2.90 (m, 4H), 2.29 (s, 3H). Mass [M+H]+:440.1

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987335B2
出典データセットuspto-grants-2015_03
ORD IDord-3799ad55235545df8ca98491a57c5750
出典メモuspto-grants-2015_03