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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 3-(Morpholine-4-sulfonyl)benzohydrazide | HCID 877246 | — |
| 反応物 | 1-(2-Chloropyridin-4-yl)ethan-1-one | HCID 13145255 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-[(E)-1-(2-chloro-4-pyridinyl)ethylideneamino]-3-morpholin-4-ylsulfonylbenzamide | HCID 72792612 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08987335B2 |
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| 出典データセット | uspto-grants-2015_03 |
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| ORD ID | ord-93fcc9e9b4b848b4ad6b6ab7c7531697 |
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| 出典メモ | uspto-grants-2015_03 |
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