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HRID 449647作成日:2026年10月24日

Potassium Phosphate, Tribasic → 6-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)pyridazin-3-amine

https://huagongshe.com/ja/reaction/449647

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物6-Bromopyridazin-3-amineHCID 2794779—
反応物2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
反応物1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridinium chlorideHCID 66742805—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒1-ButanolHCID 263—
溶媒WaterHCID 962—
生成物6-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)pyridazin-3-amineHCID 6674280882%

反応条件

温度115 °C

反応手順

In a 15 mL microwave reaction vial was added potassium phosphate tribasic (1.43 g, 6.74 mmol), 6-bromopyridazin-3-amine (335 mg, 1.93 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridinium chloride (500 mg, 1.93 mmol), X-PHOS (138 mg, 289 μmol) and bis(dibenzylideneacetone)palladium (83 mg, 144 μmol) in 7 mL n-butanol and 1.4 mL H2O. The tube was sealed under argon and heated at 115° C. in oil bath for 3 hrs then stirred at room temperature overnight. The phases were separated and the aqueous was extracted with EtOAc. (10 ml). Water (20 mL) was added to the residual aqueous phase and was extracted with DCM (3×10 mL). The extracts were combined with the EtOAc organic phase. The resultant solution was absorbed onto silica gel and purified by LC chromatography eluting with 0-10% (10% NH4OH in MeOH) in 1/1 EtOAc/hexane to afford 300 mg (82%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481540B2
出典データセットuspto-grants-2013_07
ORD IDord-cafd7974e6f74ac290c8eed5ebf44287
出典メモuspto-grants-2013_07