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HRID 42194作成日:2026年10月26日

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

https://huagongshe.com/reaction/42194

反応式

関与物質

役割名称HCID仕込み量
反応物Methyltriphenylphosphonium iodideHCID 638159—
反応物Potassium tert-butoxideHCID 23665647—
反応物1-[4-(4-Benzyl-phthalazin-1-yl)-3,4,5,6-tetrahydro-2H-[1,2]bipyrazinyl-5'-yl]-ethanoneHCID 59240632—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Benzyl-phthalazin-1-yl)-5'-isopropenyl-3,4,5,6-tetrahydro-2H-[1,2']bipyrazinylHCID 5924052878.9%

反応条件

温度5 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536168B2
出典データセットuspto-grants-2013_09
ORD IDord-ea71cd983c34410085938ee95ef21ee6
出典メモuspto-grants-2013_09