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HRID 1874522作成日:2026年10月27日

Tetrahydrofuran → N-[5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-2-fluorophenyl]-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1874522

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Thionyl ChlorideHCID 24386—
反応物1-methyl-1H-pyrazole-5-carboxylic acidHCID 643158—
反応物N-[6-(3-amino-4-fluorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749270—
触媒DimethylformamideHCID 6228—
溶媒DimethylacetamideHCID 31374—
生成物N-[5-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-2-fluorophenyl]-1-methyl-1H-pyrazole-5-carboxamideHCID 5774934367%

反応手順

In the same manner as in Example 55 and using 1-methyl-1H-pyrazole-5-carboxylic acid (50.9 mg, 0.404 mmol), tetrahydrofuran (5 mL), thionyl chloride (70.0 μL, 0.807 mmol), N,N-dimethylformamide (2 drops), N-[6-(3-amino-4-fluorophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (120 mg, 0.367 mmol) and N,N-dimethylacetamide (5 mL) as starting materials, the title compound (107 mg, 67%) was obtained as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304557B2
出典データセットuspto-grants-2012_11
ORD IDord-1d4fb44cfd964b958b2d13844d606941
出典メモuspto-grants-2012_11