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HRID 911141作成日:2026年10月26日

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl → N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amine

https://huagongshe.com/reaction/911141

反応式

関与物質

役割名称HCID仕込み量
反応物2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
反応物Sodium t-butoxideHCID 23676156—
反応物4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amineHCID 66735161—
反応物1-Chloro-6,7-dihydro-4-phenyl-5H-cyclopenta[d]pyridazineHCID 86614164—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
生成物N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amineHCID 57756249—

反応条件

温度100 °C

反応手順

A resealable reaction tube was charged with tris(dibenzylideneacetone)dipalladium (0) (0.012 g, 0.013 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (0.021 g, 0.051 mmol), 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amine (0.075 g, 0.257 mmol), 1-chloro-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazine (0.059 g, 0.257 mmol), and sodium tert-butoxide (0.035 g, 0.359 mmol). This mixture was purged with nitrogen for several minutes, followed by addition of 0.780 mL of toluene. The vial was capped and heated at 100° C. for 1.5 h. Upon cooling, ethyl acetate was added and a precipitate formed. After filtration and washing with EtOAc, the crude material was purified by ISCO silica gel chromatography (90/10/1 DCM/MeOH/NH4OH, 12 g column), to provide N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amine as a tan solid. MS m/z=487 [M+H]+. Calc'd for C30H26N6O: 486.57.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022221B2
出典データセットuspto-grants-2011_09
ORD IDord-2ce4fb20b3494e57a25d9f69d61ae3e6
出典メモuspto-grants-2011_09