참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Fluorobenzylamine | HCID 67326 | — |
| 반응물 | 3,4-Bis(benzyloxy)-6-chloropyridazine | HCID 12213474 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 촉매 | Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II) | HCID 53384307 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 5,6-bis(Benzyloxy)-N-[(4-fluorophenyl)methyl]pyridazin-3-amine | HCID 71269907 | — |
반응 단계
3,4-Bis(benzyloxy)-6-chloropyridazine (Intermediate 1) (1 g, 3.1 mmol), [1,1′-bis(di-tert-butylphosphino)ferrocene]palladium(II) dichloride (0.100 g, 0.15 mmol) and sodium tert-butoxide (0.59 g, 6.1 mmol) were added to dioxane (10.2 ml). The resulting mixture was purged with nitrogen before 4-fluorobenzylamine (78 mg, 6.1 mmol) was added. The mixture was heated at 120° C. for 1 hour under microwave irradiation. Upon cooling the crude mixture was quenched with water and extracted with ethyl acetate before the organic extracts were dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography on silica eluting with 0-100% ethyl acetate/petrol to yield the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09290456B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-9098af5f01ae4862a06b5c17d07a51ae |
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| 출처 메모 | uspto-grants-2016_03 |
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