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HRID 1966752作成日:2026年10月24日
Cesium carbonate → 5-{1-tert-Butyl-2-[2-(2,4-dimethyl-oxazol-5-yl)-phenyl]-1H-benzimidazol-5-yl}-pyrimidin-2-ylamine
https://huagongshe.com/ja/reaction/1966752
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 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | 2,4-Dimethyloxazole | HCID 138961 | — |
| 反応物 | 5-[1-tert-butyl-2-(2-iodo-phenyl)-1H-benzimidazol-5-yl]-pyrimidin-2-ylamine | HCID 58542069 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Water ethylacetate | HCID 22728543 | — |
| 生成物 | 5-{1-tert-Butyl-2-[2-(2,4-dimethyl-oxazol-5-yl)-phenyl]-1H-benzimidazol-5-yl}-pyrimidin-2-ylamine | HCID 58541930 | 41% |
反応手順
To a vial are added 5-[1-tert-butyl-2-(2-iodo-phenyl)-1H-benzimidazol-5-yl]-pyrimidin-2-ylamine (50 mg, 0.107 mmol), 2,4-dimethyl-oxazole (21 mg, 0.216 mol), palladium(II) acetate (5 mg, 0.022 mmol), PPh3 (6 mg, 0.023 mmol) and Cs2CO3 (70 mg, 0.215 mmol) in DMF (1.5 mL). The reaction mixture is stirred at 140° C. for 18 hours. The reaction mixture is diluted with EtOAc/water. The organic layer is separated, washed with brine, dried under anhydrous Na2SO4, filtered and concentrated. The residue is purified by silica gel flash column chromatography with 0-5% MeOH/CH2Cl2 as the eluent. The product fractions are collected and concentrated to afford the title compound (19 mg, 41%) as an off-white solid. LCMS (ESMS): m/z 439.86 (M++1)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08420655B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-c897844a27c649219e060d5138cf8e00 |
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| 出典メモ | uspto-grants-2013_04 |
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