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HRID 1667911作成日:2026年10月23日

Triethylamine → N-[3-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-4-methylphenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/ja/reaction/1667911

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,5-Dimethyl-2H-pyrazole-3-carbonyl chlorideHCID 2736299—
反応物N-[6-(5-amino-2-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamideHCID 57505483—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium BicarbonateHCID 516892—
生成物N-[3-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-4-methylphenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5750548864.1%

反応手順

To a solution of N-[6-(5-amino-2-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide (72.6 mg, 0.224 mmol) in tetrahydrofuran (4.0 mL) were added a solution of 1,3-dimethyl-1H-pyrazole-5-carbonyl chloride (46.3 mg, 0.29 mmol) in tetrahydrofuran (0.5 mL) and triethylamine (68 mg, 0.672 mmol) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was diluted with saturated aqueous sodium hydrogencarbonate solution, and extracted three times with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was filtrated, washed with ethyl acetate/hexane to give the title compound (64 mg, 64%) as a brown powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08044049B2
出典データセットuspto-grants-2011_10
ORD IDord-058c0fcbee3d484c9be87f6fbf08593e
出典メモuspto-grants-2011_10