참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Heptane | HCID 8900 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 4-Methylbenzylamine | HCID 66035 | — |
| 반응물 | 4,5-Bis(bromomethyl)-3,6-dichloropyridazine | HCID 57471629 | — |
| 촉매 | Tetrabutylammonium Iodide | HCID 67553 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,4-dichloro-6-(4-methoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-d]pyridazine | HCID 59240536 | 41% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08536168B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-5a00fc92a557426b89643e8e79018b9c |
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| 출처 메모 | uspto-grants-2013_09 |
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