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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2037029생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2037029

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-Amino-3-chlorobenzonitrileHCID 519896—
반응물Binap, (A+-)-HCID 634876—
반응물Tert-butyl 5-chloro-3-formyl-6-methylpyrazolo[1,5-a]pyrimidin-7-yl(cyclopropyl)carbamateHCID 86652158—
촉매palladium(II) acetateHCID 167845—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
생성물3-Chloro-4-(7-(cyclopropylamino)-3-formyl-6-methylpyrazolo[1,5-a]pyrimidin-5-ylamino)benzonitrileHCID 5831371033%

반응 단계

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)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08575177B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-0afea3ace91d40f696139dfdf22f48c7
출처 메모uspto-grants-2013_11