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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384908생성일: 2026년 10월 25일

5-Bromo-2-iodopyridine → Rac-[2-(5-bromo-pyridin-2-yl)-1-(3,4-dichloro-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/384908

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참여 물질

역할이름HCID투입량
반응물5-Bromo-2-iodopyridineHCID 593690—
반응물Rac-[(3,4-dichloro-phenyl)-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl esterHCID 87442373—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물Rac-[2-(5-bromo-pyridin-2-yl)-1-(3,4-dichloro-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl esterHCID 68409891—

반응 조건

온도0 °C

반응 단계

To a solution of 0.705 g (2.41 mmol) 5-bromo-2-iodopyridine in 4.8 ml dry tetrahydrofuran were added at 0° C. drop-wise 1.20 ml (2.41 mmol) of a 2M solution of isopropylmagnesium chloride in tetrahydrofuran. The mixture was stirred at 0° C. for 1.5 h and then 0.250 g (0.688 mmol) rac-[(3,4-Dichloro-phenyl)-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester (Intermediate 9) were added. The ice bath was removed and stirring continued at ambient temperature for 2 h. The reaction was quenched by addition of 7 ml saturated aqueous ammonium chloride solution. The mixture was diluted with water and extracted with ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered and evaporated. The crude product was purified by flash-chromatography over silica gel with a heptane/ethyl acetate gradient beginning with 5% ethyl acetate. The title compound was obtained al light yellow solid: MS (ISP): 459.1 and 461.1 (M+H)+, 403.0 and 405.1 ((M-isobutene)+H)+ (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367838B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-9ed7ea5c01f644d98cf62c9452672e31
출처 메모uspto-grants-2013_02