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HRID 49088作成日:2026年10月24日
Piperidine → 2-Oxo-3-[5-(2-pyrrolidin-1-yl-ethoxy)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-sulfonic acid amide
https://huagongshe.com/ja/reaction/49088
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 2-Oxoindoline-5-sulfonamide | HCID 10198232 | — |
| 反応物 | 5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde | HCID 22042092 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Oxo-3-[5-(2-pyrrolidin-1-yl-ethoxy)-1H-indol-2-ylmethylene]-2,3-dihydro-1H-indole-5-sulfonic acid amide | HCID 69344083 | 80% |
反応手順
A mixture of 2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide (28 mg, 0.13 mmol), 5-(2-pyrrolidin-1-yl-ethoxy)-1H-indole-2-carbaldehyde (34 mg, 0.13 mmol) and piperidine (0.1 mL) in ethanol (1 mL) was heated at 90° C. for 2 hours. The reaction was cooled at 0° C. for overnight. The precipitate was collected by vacuum filtration, washed with cold ethanol and dried to give 47 mg (80%) of the title compound as an orange solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06706709B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-22473575d84e496bb2a3edaf31178be3 |
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| 出典メモ | uspto-grants-2004_03 |
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