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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410292생성일: 2026년 10월 25일

2,5-Dihydrofuran → (1H-benzo[d]imidazol-2-yl)(4-(3-(2,3-dihydro furan-3-yl)pyridin-2-yloxy)phenyl)methanone

https://huagongshe.com/reaction/410292

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DihydrofuranHCID 15570—
반응물N-Methyl dicyclohexylamineHCID 24210—
반응물(1H-benzo[d]imidazol-2-yl)(4-(3-bromopyridin-2-yloxy)phenyl)methanoneHCID 59326957—
촉매HCID 178418851HCID 178418851—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물(1H-benzo[d]imidazol-2-yl)(4-(3-(2,3-dihydro furan-3-yl)pyridin-2-yloxy)phenyl)methanoneHCID 59326803—
생성물(1H-benzo[d]imidazol-2-yl)(4-(3-(2,3-dihydrofuran-2-yl)pyridin-2-yloxy)phenyl)methanoneHCID 59327153—

반응 조건

온도80 °C

반응 단계

A mixture of (1H-benzo[d]imidazol-2-yl)(4-(3-bromopyridin-2-yloxy)phenyl)methanone (1.522 g, 3.86 mmol), 2,5-dihydrofuran (1.400 mL, 18.98 mmol, Aldrich), N-cyclohexyl-N-methylcyclohexanamine (1.600 mL, 7.54 mmol, Aldrich) and bis(tri-tert-butylphosphine)palladium (0) (0.194 g, 0.380 mmol, Strem) in dioxane (10 mL) was sealed in a microwave vessel under an atmosphere of argon and heated thermally at 80° C. for 6 h. The reaction was diluted with EtOAc and the mixture was extracted with water (1×) and brine (1×). The organic mixture was evaporated onto silica gel and purified by flash chromatography (Isco (120 gram)) eluting with EtOAc:hexanes (0:1→1:2) to give 650 mg of (1H-benzo[d]imidazol-2-yl)(4-(3-(2,3-dihydrofuran-2-yl)pyridin-2-yloxy)phenyl)methanone and 325 mg of (1H-benzo[d]imidazol-2-yl)(4-(3-(2,3-dihydro furan-3-yl)pyridin-2-yloxy)phenyl)methanone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759532B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-ae7d634543124ef5bb91d81aeaf0ab07
출처 메모uspto-grants-2014_06