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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257생성일: 2026년 10월 23일

2-Chloropyrimidine → N-[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]pyrimidin-2-amine

https://huagongshe.com/ko/reaction/257

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloropyrimidineHCID 74404—
반응물3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
시약Cesium carbonateHCID 10796—
촉매2-(Dicyclohexylphosphino)biphenylHCID 2734216—
촉매Palladium (II) acetateHCID 4144353—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]pyrimidin-2-amineHCID 6879035918.78%

반응 조건

온도100 °C

반응 단계

2-Chloropyrimidine (0.056 g, 0.49 mmol), 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline (0.100 g, 0.49 mmol), Palladium acetate (0.011 g, 0.05 mmol), 2-(Dicyclohexylphosphino)biphenyl (0.017 g, 0.05 mmol) and Cesium carbonate (0.481 g, 1.48 mmol) were placed in a microwave vial. The mixture was capped and flushed with argon. 1,2-dimethoxyethane (5 mL) was added and the mixture was run in a microwave for 60 minutes at 100°C. Very little product. Added 0.1 eq ligand and palladium acetate, flushed with argon and run in the microwave at 100°C for 60 min. No change. Seems as if the 2-chloropyrimidine is not very soluble in DME. Added 1.5 mL DMF and the reaction was run again in the microwave for 60 minutes. The reaction mixture was filtrated through Celite and washed with dichloromethane. The filtrate was concentrated and the crude product was purified by preparative chromatography. The productcontaining fractions were pooled, concentrated and the residue was partitioned between sat. NaHCO3 (aq) and dichloromethane. The organic layer was separated by a Phase Separator and concentrated giving N-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl)pyrimidin-2-amine (0.026 g, 18.78 %).

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-20ba80f324544fc48cbce515702585f3
출처 메모750 AstraZeneca ELN dataset