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HRID 645491作成日:2026年10月26日
HOAt → 2-Cyano-4-(cyclohexylmethylamino)pyrimidine-5-carboxylic acid(2-morpholin-4-yl-1-phenylethyl)amide
https://huagongshe.com/reaction/645491
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | HOAt | HCID 181649 | — |
| 反応物 | 2-(Morpholin-4-yl)-1-phenylethan-1-amine | HCID 2814462 | — |
| 反応物 | 2-Cyano-4-(cyclohexylmethylamino)-pyrimidine-5-carboxylic acid | HCID 68703380 | — |
| 反応物 | EDCl H2O | HCID 87672115 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-Cyano-4-(cyclohexylmethylamino)pyrimidine-5-carboxylic acid(2-morpholin-4-yl-1-phenylethyl)amide | HCID 57580377 | — |
反応手順
To a solution of 2-cyano-4-(cyclohexylmethylamino)-pyrimidine-5-carboxylic acid (0.33 mmol, step 1.4) in DMF (2.0 mL) are added 2-morpholin-4-yl-1-phenylethylamine (69 mg, step 1.3), EDCl—H2O (0.50 mmol) and HOAt (0.50 mmol) at room temperature. After stirring at room temperature for 24 h, the reaction mixture is diluted with AcOEt. The mixture is washed with water, dried over Na2SO4, filtered, and concentrated in vacuo. The resulting residue is purified by RP-HPLC to give the title compound; 1H NMR (DMSO) δ 0.6-1.08 (m, 2H), 1.20-1.35 (m, 3H), 1.65-1.78 (m, 6H), 2.48-2.53 (m, 2H), 2.60-2.62 (m, 2H), 2.87-2.93 (m, 2H), 3.31-3.35 (m, 1H), 3.36-3.44 (M, 1H), 3.60-3.68 (m, 4H), 5.29-5.35 (m, 1H), 7.34-7.36 (m, 1H), 7.43-7.47 (m, 2H), 7.50-7.52 (m, 2H), 8.86 (s, 1H), 9.00-9.04 (m, 1H), 9.21 (d, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07704996B2 |
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| 出典データセット | uspto-grants-2010_04 |
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| ORD ID | ord-aef23442ebd141288d5b04ce6fa32f44 |
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| 出典メモ | uspto-grants-2010_04 |
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