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HRID 38863作成日:2026年10月25日
Sodium Iodide → 6-(1H-Indol-4-yl)-4-[5-({4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}methyl)-1,3,4-oxadiazol-2-yl]-1H-indazole
https://huagongshe.com/reaction/38863
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 4-(2-Piperazin-1-yl-ethyl)-morpholine | HCID 2734640 | — |
| 反応物 | 4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole | HCID 66776954 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 6-(1H-Indol-4-yl)-4-[5-({4-[2-(4-morpholinyl)ethyl]-1-piperazinyl}methyl)-1,3,4-oxadiazol-2-yl]-1H-indazole | HCID 66776781 | 50.5% |
反応手順
4-[2-(1-piperazinyl)ethyl]morpholine (14.1 mg, 0.11 mmol) and 4-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole (50 mg, 0.102 mmol) were dissolved in acetonitrile (0.5 ml) and N,N-diisopropylethylamine (0.026 ml, 0.15 mmol) was added, followed by sodium iodide (15.3 mg, 0.102 mmol). The solution was stirred at 70° C. for 18 h and blown to dryness under a stream of nitrogen. Isopropanol (0.3 ml) was added followed by 2M sodium hydroxide (0.3 ml) and stirred for 5 h when the mixture was neutralised and the solvent removed under a stream of nitrogen. The crude product was dissolved in dimethylsulphoxide (0.3 ml) and methanol (0.15 ml) with formic acid (0.05 ml) then purified by Mass Directed Automated Preparative HPLC (Method F) to give the title compound (26.4 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524751B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-a395d4ab713344a8a1db6a2018ac61b2 |
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| 出典メモ | uspto-grants-2013_09 |
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