関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Resorcinol | HCID 5054 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 6-Bromo-4-chloro-7H-pyrrolo[2,3-D]pyrimidine | HCID 45789827 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 3-[(6-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy]phenol | HCID 69490171 | 32.7% |
反応手順
6-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (100 mg, 0.41 mmol), prepared as in reference 1, is mixed with resorcinol (451 mg, 4.1 mmol) and diisopropylethylamine (714 μL, 4.1 mmol) in dioxane (1.3 mL). The mixture is heated to 150° C. for 3 days, with stirring. The reaction is then cooled to ambient temperature and the solvent is removed. The resultant crude product is purified by flash column chromatography using a gradient of 3-5% MeOH in DCM to yield 5-(6-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yloxyl)-phenol (41 mg; 32%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07253166B2 |
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| 出典データセット | uspto-grants-2007_08 |
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| ORD ID | ord-921ea4bdc99d4bf68bd35b95ceda85f6 |
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| 出典メモ | uspto-grants-2007_08 |
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