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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 927096생성일: 2026년 10월 27일

4-Fluorobenzylamine → 5,6-bis(Benzyloxy)-N-[(4-fluorophenyl)methyl]pyridazin-3-amine

https://huagongshe.com/reaction/927096

반응식

참여 물질

역할이름HCID투입량
반응물4-FluorobenzylamineHCID 67326—
반응물3,4-Bis(benzyloxy)-6-chloropyridazineHCID 12213474—
반응물Sodium t-butoxideHCID 23676156—
촉매Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
용매1,4-DioxaneHCID 31275—
생성물5,6-bis(Benzyloxy)-N-[(4-fluorophenyl)methyl]pyridazin-3-amineHCID 71269907—

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290456B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-9098af5f01ae4862a06b5c17d07a51ae
출처 메모uspto-grants-2016_03