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HRID 1476412作成日:2026年10月25日
5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridine → Methyl 1-isopropyl-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-indazole-4-carboxylate
https://huagongshe.com/reaction/1476412
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridine | HCID 24208789 | — |
| 反応物 | Methyl 6-bromo-1-isopropyl-3-methyl-1H-indazole-4-carboxylate | HCID 67466747 | — |
| 生成物 | Methyl 1-isopropyl-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-indazole-4-carboxylate | HCID 67467136 | — |
反応手順
The title compound was prepared in the same manner as described for example 35 (step a) from methyl 6-bromo-1-isopropyl-3-methyl-1H-indazole-4-carboxylate (1 g, 3.36 mmol) and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine (0.98 g, 4.04 mmol) wherein the reaction mixture was stirred at 100° C. for 5 h. The product was collected as an off white solid (600 mg, 53%). LCMS (ES−) m/z: 333.08.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09018382B2 |
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| 出典データセット | uspto-grants-2015_04 |
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| ORD ID | ord-1f62eb6f9a164d15845f2aa07e9cdb72 |
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| 出典メモ | uspto-grants-2015_04 |
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