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HRID 877603作成日:2026年10月26日

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

https://huagongshe.com/reaction/877603

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-(2-Chloropyridin-4-yl)ethan-1-oneHCID 13145255—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物N-[(E)-1-(2-chloro-4-pyridinyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamideHCID 7279261260%

反応条件

温度120 °C

反応手順

1-(2-Chloropyridin-4-yl)ethanone (20 mg, 0.129 mmol) and 3-(morpholinosulfonyl)benzohydrazide (36.7 mg, 0.129 mmol) were dissolved in methanol (4 mL) in the presence of acetic acid as a catalyst, and the reaction mixture was heated via microwave irradiation to 120° C. for 30 min. Following cooling, the solvent was removed by vacuum and the resulting crude material was purified by flash column chromatography affording the title compound in a 60% yield. 1H NMR (400 MHz, CDCl3): δ 9.43 (m, 1H), 8.39 (m, 2H), 8.15 (d, 1H, J=8.0 Hz), 7.93 (d, 1H, J=7.6 Hz), 7.70 (t, 1H, J=7.6 Hz), 7.52 (m, 1H), 3.73 (m, 4H), 3.02 (m, 4H), 2.35 (s, 3H). ESI-MS: 423.1 [M+H]+.

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-93fcc9e9b4b848b4ad6b6ab7c7531697
出典メモuspto-grants-2015_03