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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606생성일: 2026년 10월 23일

N-(5-amino-4-fluoro-2-methylphenyl)acetamide → N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-4-fluoro-2-methylphenyl]acetamide

https://huagongshe.com/ko/reaction/606

반응식

참여 물질

역할이름HCID투입량
반응물N-(5-amino-4-fluoro-2-methylphenyl)acetamideHCID 89099132—
반응물5-Chloro-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 89827173—
시약Cesium carbonateHCID 10796—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매Di-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
용매1,4-DioxaneHCID 31275—
생성물N-[5-[[3-cyano-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidin-5-yl]amino]-4-fluoro-2-methylphenyl]acetamideHCID 7216392620.63%

반응 조건

온도150 °C

반응 단계

In 20 ml microwave vial were added 5-chloro-7-(cyclopropylamino)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (200 mg, 0.86 mmol), N-(5-amino-4-fluoro-2-methylphenyl)acetamide (164 mg, 0.90 mmol), Pd2dba3 (39.2 mg, 0.04 mmol), di-tert- butyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (37.5 mg, 0.09 mmol) and Cs2CO3 (837 mg, 2.57 mmol). The vessel was fitted with septum, gas inlet and dioxane (8 mL) was added via syringe. The resulting suspension was stirred for 5 min. under N2. The septum and gas inlet quickly replaced with microwave vial cap and the mixture was heated to 150oC under microwave irradiation for 30 min. The reaction mixture filtered through celite, filtrate concentrated, combined with EN02368-53 experiment and purified by ISCO column (0-5% MeOH-CH2Cl2). The obtained compound triturated with CH3CN, filtered and dried to give light brown color solid. Conclusion: product isolated

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-71ad501d78264f9aa8b8fb6c66e7e044
출처 메모750 AstraZeneca ELN dataset