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HRID 1167778作成日:2026年10月27日
Cesium carbonate → N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-2-thiomorpholin-4-yl-isonicotinamide
https://huagongshe.com/reaction/1167778
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Thiomorpholine | HCID 67164 | — |
| 反応物 | 2-bromo-N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-isonicotinamide | HCID 22993429 | — |
| 生成物 | N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-2-thiomorpholin-4-yl-isonicotinamide | HCID 22993436 | 55.4% |
反応手順
A stirred suspension of 500 mg (1.11 mmol) 2-bromo-N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-isonicotinamide. 1.5 g (11.1 mmol) thiomorpholine and 725 mg (2.23 mmol) cesium carbonate in a thick-walled glass pressure tube fitted with a teflon cap was heated at 140° C. for 48 h. The reaction mixture was then cooled to room temperature and poured onto water. The mixture was extracted three times with ethyl acetate, and the combined organic phases were washed with saturated brine, dried over sodium sulfate, and concentrated in vacuo. Flash chromatography (1/99 methanol/dichloromethane) followed by trituration in ether/ethyl acetate/hexane afforded 290 mg (55%) N-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-2-thiomorpholin-4-yl-isonicotinamide as an off-white crystalline solid. ES-MS m/e (%)): 472 (M+H+, 100).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06620811B2 |
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| 出典データセット | uspto-grants-2003_09 |
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| ORD ID | ord-f64c3976f07d4022834548f037e2b5b1 |
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| 出典メモ | uspto-grants-2003_09 |
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