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HRID 226010作成日:2026年10月26日

Cesium carbonate → 8-(1-Ethyl-propyl)-2,6-dimethyl-3-(3-methyl-benzo[b]thiophen-2-yl)-imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/226010

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物TriphenylphosphineHCID 11776—
反応物3-Methylbenzo[b]thiopheneHCID 73817—
反応物8-(1-Ethyl-propyl)-3-iodo-2,6-dimethyl-imidazo[1,2-b]pyridazineHCID 57752681—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒DimethylformamideHCID 6228—
生成物8-(1-Ethyl-propyl)-2,6-dimethyl-3-(3-methyl-benzo[b]thiophen-2-yl)-imidazo[1,2-b]pyridazineHCID 5775262580%

反応条件

温度130 °C

反応手順

A mixture of 8-(1-ethyl-propyl)-3-iodo-2,6-dimethyl-imidazo[1,2-b]pyridazine (0.145 mmol), 3-methyl-benzothiophene (7.25 mmol), Pd2 dba3 (0.0072 mmol), triphenylphosphine (0.029 mmol), and cesium carbonate (0.29 mmol) in previously degassed DMF (0.5 ml) is added to a pressure tube with a stirring bar. Mixture is degassed for 30 min. After heating for 16 h at 130° C., the reaction mixture is cooled, diluted with diethylether and washed with saturated aqueous ammonium chloride solution. The organic layer is dried over anhydrous magnesium sulfate, filtered, and the solvent is removed in vacuo. The residue is purified by silica gel column chromatography using mixtures of hexane-ethyl acetate as eluent to give the title compound (80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557103B2
出典データセットuspto-grants-2009_07
ORD IDord-43ac9d937e5c4f608cbb04b3b604d3a8
出典メモuspto-grants-2009_07