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HRID 60817作成日:2026年10月25日
(Bis(2-methoxyethyl)amino)sulfur trifluoride → N-((5-fluoro-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide
https://huagongshe.com/reaction/60817
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (Bis(2-methoxyethyl)amino)sulfur trifluoride | HCID 2734690 | — |
| 反応物 | N-((5-hydroxy-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide | HCID 71715162 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-((5-fluoro-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide | HCID 71715220 | — |
反応手順
A solution of N-((5-hydroxy-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide (0.07 mmol, 0.036 g) in DCM (0.3 mL) was added to a mixture of bis(2-methoxyethyl)aminosulfur trifluoride (0.14 mmol, 0.027 mL) in DCM (0.2 mL) at −78° C. under argon. The resulting mixture was stirred at −78° C. for 1 h and at rt for another 1.5 h. The desired product was purified by preparative TLC to give N-((5-fluoro-1-(2-methyl-4-phenylthiazole-5-carbonyl)piperidin-2-yl)methyl)quinoline-8-carboxamide with unidentified stereochemistry (Y: 16%). MS (ESI) 489 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09440982B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-5080850ddb214b1684fe9feaad436637 |
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| 出典メモ | uspto-grants-2016_09 |
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