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HRID 1874441作成日:2026年10月27日

Tetrahydrofuran → N-[3-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)phenyl]-1-ethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1874441

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Oxalyl chlorideHCID 65578—
反応物1-Ethyl-1H-pyrazole-5-carboxylic acidHCID 565702—
反応物N-[6-(3-aminophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamideHCID 57749117—
触媒DimethylformamideHCID 6228—
溶媒DimethylacetamideHCID 31374—
生成物N-[3-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)phenyl]-1-ethyl-1H-pyrazole-5-carboxamideHCID 5774925783%

反応手順

In the same manner as in Example 18-4 and using 1-ethyl-1H-pyrazole-5-carboxylic acid (269 mg, 1.92 mmol), tetrahydrofuran (7 mL), oxalyl chloride (169 μL, 1.94 mmol), N-[6-(3-aminophenoxy)[1,2,4]triazolo[1,5-a]pyridin-2-yl]cyclopropanecarboxamide (200 mg, 0.646 mmol), N,N-dimethylformamide (1 drop) and N,N-dimethylacetamide (3 mL) as starting materials, the title compound (231 mg, 83%) 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-ace393ec6eec4b7b9ae74d4d9caa80bf
出典メモuspto-grants-2012_11