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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42194생성일: 2026년 10월 25일

Methyltriphenylphosphonium iodide → 4-(4-Benzyl-phthalazin-1-yl)-5'-isopropenyl-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinyl

https://huagongshe.com/reaction/42194

반응식

참여 물질

역할이름HCID투입량
반응물Methyltriphenylphosphonium iodideHCID 638159—
반응물Potassium tert-butoxideHCID 23665647—
반응물1-[4-(4-Benzyl-phthalazin-1-yl)-3,4,5,6-tetrahydro-2H-[1,2]bipyrazinyl-5'-yl]-ethanoneHCID 59240632—
용매TetrahydrofuranHCID 8028—
생성물4-(4-Benzyl-phthalazin-1-yl)-5'-isopropenyl-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinylHCID 5924052878.9%

반응 조건

온도5 °C

반응 단계

Methyltriphenylphosphonium iodide (115 mg, 0.28 mmol) is dissolved in THF (750 μL) and chilled to 5° C. While stirring add potassium t-butoxide (310 μL, 1M in THF, 0.31 mmol) to the solution. After 30 minutes add the mixture to a solution of 1-[4-(4-Benzyl-phthalazin-1-yl)-3,4,5,6-tetrahydro-2H-[1,2]bipyrazinyl-5′-yl]-ethanone (100 mg, 0.24 mmol) and THF (750 μL). Stir 30 minutes. Analysis shows 60-70% completion. A second portion of methyl triphenyl phosphonium iodide (115 mg, 0.28 mmol) is dissolved in THF (750 μl) and chilled to 5° C. While stirring add potassium t-butoxide (310 μL, 1M in THF, 0.31 mmol) to the solution. Again add this mixture to the current reaction. Reaction quickly proceeds to completion. Quench by adding saturated ammonium chloride. Concentrate in vacuo to remove THF and partition between water and EtOAc. Extract with EtOAc, and wash combined organics with brine. Concentrate EtOAc in vacuo. The residue is purified by flash chromatography on silica gel (EtOAc/Heptane) to afford the title compound (80 mg, 78%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536168B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ea71cd983c34410085938ee95ef21ee6
출처 메모uspto-grants-2013_09