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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 278생성일: 2026년 10월 24일

2-Chloro-4-aminopyrimidine → 2-chloro-N-pyridin-4-ylpyrimidin-4-amine

https://huagongshe.com/ko/reaction/278

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-4-aminopyrimidineHCID 345752—
반응물4-IodopyridineHCID 609492—
시약Cesium carbonateHCID 10796—
촉매Palladium (II) acetateHCID 4144353—
촉매(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
용매1,4-DioxaneHCID 31275—
생성물2-chloro-N-pyridin-4-ylpyrimidin-4-amineHCID 2230968645.34%

반응 조건

온도80 °C

반응 단계

diacetoxypalladium (0.035 g, 0.15 mmol) was added to a mixture of 2-chloropyrimidin-4-amine (0.250 g, 1.93 mmol), 4-iodopyridine (0.396 g, 1.93 mmol), cesium carbonate (0.755 g, 2.32 mmol) and (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (0.105 g, 0.19 mmol) in 1,4-dioxane (10 mL) and the reaction mixture stirred for 18 hours at 80 °C under nitrogen. EtOAc (50ml) was added to the reaction mixture and then the organics washed with water (3 x 50ml), brine (50ml) and then dried over MgSO4. The organics were then evaporated in vacuo to give the crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Pure fractions were evaporated to dryness to afford 2-chloro-N-(pyridin-4-yl)pyrimidin-4-amine (0.181 g, 45.3 %) as an orange solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-0cc10dc98bd741d3bb43f77d99dd2224
출처 메모750 AstraZeneca ELN dataset