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HRID 1800412作成日:2026年10月27日

Cyclopropanecarbonyl chloride → Tert-butyl [3-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-4-methylphenyl]carbamate

https://huagongshe.com/reaction/1800412

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclopropanecarbonyl chlorideHCID 77637—
反応物Tert-butyl {3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-4-methylphenyl}carbamateHCID 57749391—
溶媒WaterHCID 962—
溶媒DimethylacetamideHCID 31374—
生成物Tert-butyl [3-({2-[(cyclopropylcarbonyl)amino][1,2,4]triazolo[1,5-a]pyridin-6-yl}oxy)-4-methylphenyl]carbamateHCID 5774928489%

反応手順

To a solution of tert-butyl{3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-4-methylphenyl}carbamate (1.50 g, 4.22 mmol) in N,N-dimethylacetamide (5 mL) was added with stirring cyclopropanecarbonyl chloride (1.15 mL, 12.7 mmol) under ice-cooling, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the insoluble material was filtered off. The filtrate was concentrated under reduced pressure, and the residue was collected by filtration and washed with ethyl acetate and hexane to give the title compound (1.59 g, 89%) as a white compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08344135B2
出典データセットuspto-grants-2013_01
ORD IDord-52842c56ed5d4060ac1f3020a31c13db
出典メモuspto-grants-2013_01