関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Chloro-6,7-dimethoxyquinazoline | HCID 2769364 | — |
| 反応物 | 3-Iodooxetane | HCID 13356686 | — |
| 試薬 | Hydrogen Peroxide | HCID 784 | — |
| 試薬 | Sulfuric Acid | HCID 1118 | — |
| 触媒 | CID 516917 | HCID 516917 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | HCID 178486894 | HCID 178486894 | 36% |
反応手順
H2O2 (30% in H2O; 153 μL, 1.5 mmol) was added dropwise over 1-2 min to a stirred solution of 4-chloro-6,7-dimethoxyquinazoline 1j (112 mg, 0.5 mmol), concentrated H2SO4 (54 μL, 1.0 mmol), 3-iodooxetane (183 mg, 1.0 mmol) and iron(II) sulfate heptahydrate (42 mg, 0.15 mmol) in DMSO (5 mL) at 60 °C. After 1-2 min a further portion of iron(II) sulfate heptahydrate (42 mg, 0.15 mmol) was added and the mixture was stirred at 60 °C for 30 min. Further H2O2 (153 μL, 1.5 mmol) and iron(II) sulfate heptahydrate (42 mg, 0.15 mmol) was added, and the mixture was stirred at 60 °C for 30 min. After allowing to cool, the mixture was poured into a 0.2 M solution of NaOH saturated with solid NaCl (30 mL) and Et2O (50 mL). The aqueous and organic layers were partitioned and the aqueous layer was extracted with Et2O (2 x 25 mL). The combined organic extracts were washed with brine (1 x 30 mL), dried (MgSO4), filtered and the solvent removed under vacuum to leave a crude oil. The oil was purified by preparative thin-layer chromatography using MeOH / EtOAc (1:9) as eluent to give the desired product 2j (47 mg, 36%).
情報源と証拠
| DOI | 10.1021/jo9010624 |
|---|
| 出典データセット | Minisci dataset from Roche |
|---|
| ORD ID | ord-c7dc4cde28854c6884a7d939870115c9 |
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| 出典メモ | Minisci dataset from Roche |
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