関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Heptane | HCID 8900 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 4-Methylbenzylamine | HCID 66035 | — |
| 反応物 | 4,5-Bis(bromomethyl)-3,6-dichloropyridazine | HCID 57471629 | — |
| 触媒 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazine | HCID 59240536 | 41% |
反応手順
To a suspension of 4,5-bis(bromomethyl)-3,6-dichloropyridazine (800 mg, 2.39 mmol) in 40 mL anhydrous THF was added with sodium carbonate (507 mg, 4.78 mmol) and tetrabutylammonium iodide (88.3 mg, 0.24 mmol). The reaction mixture was added with 4-methylbenzylamine (0.31 mL, 2.39 mmol) in 20 mL THF dropwisely for 2 h. The reaction mixture was heated at 70° C. for 8 h and concentrated. The crude material was dissolved in DCM and washed with water and brine. The organic solution was dried over Na2SO4 and concentrated to afford a crude oil. The mixture was purified by flash chromatography on silica gel, eluting with 10-80% EtOAc:heptane to afford a off-white solid (300 mg, yield: 41%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08536168B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-5a00fc92a557426b89643e8e79018b9c |
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| 出典メモ | uspto-grants-2013_09 |
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