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HRID 74288作成日:2026年10月25日
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2-(3-Acetylaminophenyl)-5-(5-chlorobenzoxazol-2-yl)-1-(tetrahydropyran-4-yl)benzimidazole
https://huagongshe.com/reaction/74288
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 反応物 | 3-Acetamidobenzoic acid | HCID 48847 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 5-Chloro-2-(2-(tetrahydropyran-4-yl)aminoanilin-5-yl)benzoxazole | HCID 67498421 | — |
| 触媒 | Methanesulfonic Acid | HCID 6395 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(3-Acetylaminophenyl)-5-(5-chlorobenzoxazol-2-yl)-1-(tetrahydropyran-4-yl)benzimidazole | HCID 67498798 | 14.3% |
反応手順
To a solution of 5-chloro-2-(2-(tetrahydropyran-4-yl)aminoanilin-5-yl)benzoxazole (see Working Example 100-2) (250 mg, 0.727 mmol) in dimethylformamide (5 mL) was added 3-acetamidobenzoic acid (130 mg, 0.727 mmol) and WSC (167 mg, 0.872 mmol), and this was stirred at room temperature for 23 hours. Saturated aqueous sodium hydrogen carbonate solution was added, the precipitated crystals were filtered, washed with water and then dried. To a solution of the residue obtained in dioxane (5 mL) was added methanesulfonic acid (2 drops), and this was heated to reflux for 3 hours. After the reaction was complete, saturated aqueous sodium hydrogen carbonate solution was added, the precipitated crystals were filtered, washed with water and then dried. The residue obtained was purified by silica gel column chromatography to yield the title compound (50.5 mg, 14%) as white crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829035B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-c614abdbba7f476ea7943da8ace5a6cf |
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| 出典メモ | uspto-grants-2014_09 |
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