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HRID 231512作成日:2026年10月27日

Triethylsilane → 4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide

https://huagongshe.com/reaction/231512

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylsilaneHCID 12052—
反応物Potassium HydroxideHCID 14797—
反応物4,5-Dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 2737093—
溶媒Trifluoroacetic acidHCID 6422—
生成物4,5,6,7-Tetrahydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 135621397—

反応条件

温度60 °C

反応手順

A solution of 3.44 g of 4,5-dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carboxamide (Ex. 24) in 40 ml of trifluoroacetic acid was stirred under nitrogen and heated to 60° C. in an oil bath. Then 5.0 ml of triethylsilane was added and the mixture was stirred at 60° C. for 24 hours. The reaction mixture was cooled and carefully poured into a beaker containing a 25% aqueous solution of potassium hydroxide and cracked ice. The product which precipitated was extracted into chloroform. The chloroform was washed with water, dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo and gave crystals which were recrystallized from toluene-hexane to give the desired product, mp 152°-154° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04847256
出典データセットuspto-grants-1989_07
ORD IDord-eec79a0350064775b60e18124d16bc30
出典メモuspto-grants-1989_07