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HRID 1668035作成日:2026年10月25日

Dimethylformamide → 3-tert-butyl-N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1668035

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-tert-butyl-1-methyl-1H-pyrazole-5-carboxylic acidHCID 720529—
反応物N-[6-(3-amino-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamideHCID 57505476—
溶媒TetrahydrofuranHCID 8028—
溶媒DimethylacetamideHCID 31374—
生成物3-tert-butyl-N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1-methyl-1H-pyrazole-5-carboxamideHCID 5750558641%

反応手順

Using 3-tert-butyl-1-methyl-1H-pyrazole-5-carboxylic acid (61 mg, 0.33 mmol), tetrahydrofuran (1.8 mL), N,N-dimethylformamide (30 μL, 0.39 mmol), oxalyl chloride (44 μL, mmol), N-[6-(3-amino-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide (90 mg, 0.28 mmol) and N,N-dimethylacetamide (1.8 mL), and in the same manner as in Example 119, the title compound (55 mg, 41%) was obtained as a white 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-46b219ee2a6d42dc9a82b1bf0faca064
出典メモuspto-grants-2011_10