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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 361생성일: 2026년 10월 23일

2,4-Dichloropyridine → N-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amine

https://huagongshe.com/ko/reaction/361

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참여 물질

역할이름HCID투입량
반응물2,4-DichloropyridineHCID 33515—
반응물2-AminooxazoleHCID 558521—
시약Potassium Phosphate, TribasicHCID 62657—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물N-(4-chloro-2-pyridinyl)-1,3-oxazol-2-amineHCID 1300162600%

반응 조건

온도160 °C

반응 단계

Objective: Will increased catalyst loading lead to increased isolated yield of the desired product? 2,4-dichloropyridine (0.109 mL, 1.01 mmol), oxazol-2-amine (102 mg, 1.22 mmol), TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (186 mg, 0.20 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (352 mg, 0.61 mmol) (Xantphos) and potassium phosphate (430 mg, 2.03 mmol) were added to a microwave vail and the vial was purged with nitrogen. Degassed dioxane (4mL) was then added and the reaction mixture was heated to 160 °C for 6 h under microwave irradiation. Dichloromethane (10 mL) was added to the crude reaction mixture and the mixture was adsorbed onto silica gel. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in heptane. Unfortunately and somewhat surprisingly, none of the desired product was isolated, although only a trace of required product was observed in the LCMS of the crude reaction mixture. Conclusion: It appears that under this higher catalyst loading the reaction is less efficent, potentially a concentration effect?

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-4973899cb35d49cd8a53a56048cd33f7
출처 메모750 AstraZeneca ELN dataset