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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 728생성일: 2026년 10월 24일

2-Acetylamino-4-aminotoluene → N-[5-[[3-cyano-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]acetamide

https://huagongshe.com/ko/reaction/728

반응식

참여 물질

역할이름HCID투입량
반응물2-Acetylamino-4-aminotolueneHCID 79492—
반응물HCID 178418222HCID 178418222—
시약Cesium carbonateHCID 10796—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
용매DimethylacetamideHCID 31374—
생성물N-[5-[[3-cyano-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-2-methylphenyl]acetamideHCID 7216428716.54%

반응 조건

온도145 °C

반응 단계

In a microwave tube, was Cs2CO3 (0.522 g, 1.60 mmol), N-(5-amino-2-methylphenyl)acetamide (0.132 g, 0.80 mmol), Pd2dba3 (0.037 g, 0.04 mmol),5-chloro-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (0.200 g, 0.80 mmol),di-tert- butyl(2',4',6'-triisopropyl-[1,1'-biphenyl]-2-yl)phosphine (0.034 g, 0.08 mmol). anhydrous DMA (2.0 mL) was added. The resulting mixture was bubbled through N2. Then the tube was capped. under microwave 145C for 30min. This reaction was repeated at 150mg again. The two batches were combined to workup The mixture was concentrated to dryness. Water (20 mL) was added. it was extracted with 10% MeOH in EtOAc, The combined organic phases were dried over Na2SO4, filtered and concentrated to dryness. It was purified by chromatography )Hex to 50% etAOc in Hex to EtOAc to 5% MeOH in EtOAc) to collect the pure product to give the product (86mg, 16.5% from total 350mg SM 5-chloro-7-(oxetan-3-ylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrile) which was washed with EtOAc and dried under a high vacuum at 60C for 16h as an offwhite solid

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-ee0c75ae423d4c13a290870b1caf79ed
출처 메모750 AstraZeneca ELN dataset