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HRID 2391367作成日:2026年10月26日

Dimethylformamide → N-(5-{[2-(acetylamino)imidazo[1,2-b]pyridazin-6-yl]oxy}-2-fluorophenyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/2391367

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物3-ethyl-1-methyl-1H-pyrazole-5-carboxylic acidHCID 820565—
反応物N-[6-(3-amino-4-fluorophenoxy)imidazo[1,2-b]pyridazin-2-yl]acetamideHCID 57505595—
溶媒TetrahydrofuranHCID 8028—
溶媒DimethylacetamideHCID 31374—
生成物N-(5-{[2-(acetylamino)imidazo[1,2-b]pyridazin-6-yl]oxy}-2-fluorophenyl)-3-ethyl-1-methyl-1H-pyrazole-5-carboxamideHCID 5750560650.1%

反応手順

Using 3-ethyl-1-methyl-1H-pyrazole-5-carboxylic acid (215 mg, 1.39 mmol), tetrahydrofuran (4.5 mL), N,N-dimethylformamide (30 μL, 0.39 mmol), oxalyl chloride (122 μL, 1.39 mmol), N-[6-(3-amino-4-fluorophenoxy)imidazo[1,2-b]pyridazin-2-yl]acetamide (300 mg, 1.00 mmol) and N,N-dimethylacetamide (6.0 mL), and in the same manner as in Example 238, the title compound (219 mg, 50%) was obtained as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273741B2
出典データセットuspto-grants-2012_09
ORD IDord-386bc339c2ec455e889bb385dfc3ca5d
出典メモuspto-grants-2012_09