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HRID 2037029作成日:2026年10月25日

Cesium carbonate → 3-Chloro-4-(7-(cyclopropylamino)-3-formyl-6-methylpyrazolo[1,5-a]pyrimidin-5-ylamino)benzonitrile

https://huagongshe.com/reaction/2037029

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-Amino-3-chlorobenzonitrileHCID 519896—
反応物Binap, (A+-)-HCID 634876—
反応物HCID 86652158HCID 86652158—
触媒palladium(II) acetateHCID 167845—
溶媒Diethyl EtherHCID 3283—
溶媒1,4-DioxaneHCID 31275—
生成物3-Chloro-4-(7-(cyclopropylamino)-3-formyl-6-methylpyrazolo[1,5-a]pyrimidin-5-ylamino)benzonitrileHCID 5831371033%

反応手順

To 4-amino-3-chlorobenzonitrile (52 mg, 0.34 mmol), Cs2CO3 (130 mg, 0.4 mmol) were added to tert-butyl 5-chloro-3-formyl-6-methylpyrazolo[1,5-a]pyrimidin-7-yl(cyclopropyl)carbamate (100 mg, 0.29 mmol) dissolved in 1,4-dioxane (1.1 mL). Racemic BINAP (11 mg, 0.017 mmol) and palladium(II) acetate (8 mg, 0.011 mmol) were then added. The mixture was sealed and irradiated at 110° C. for 60 min in the microwave. Et2O (3 mL) was added and the solution was filtered. The filtrate was concentrated in vacuo. The crude residue was dissolved in dichloromethane (1.5 mL) and trifluoroacetic acid (1.5 mL). After stirring at room temperature for 1 hour, the solution was concentrated under a stream of air. The crude material was purified by silica gel chromatography (3% acetone/dichloromethane) to yield the product, 3-chloro-4-(7-(cyclopropylamino)-3-formyl-6-methylpyrazolo[1,5-a]pyrimidin-5-ylamino)benzonitrile (34 mg, 33% yield). LCMS (M+1=367)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08575177B2
出典データセットuspto-grants-2013_11
ORD IDord-0afea3ace91d40f696139dfdf22f48c7
出典メモuspto-grants-2013_11