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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1926010생성일: 2026년 10월 25일

4-chloro-5H-pyrrolo[3,2-d]pyrimidine → [2-(benzyloxy)-5-(5H-pyrrolo[3,2-d]pyrimidin-4-ylamino)phenyl]methanol

https://huagongshe.com/reaction/1926010

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참여 물질

역할이름HCID투입량
반응물4-chloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5370695—
반응물4-Benzyloxy-3-hydroxymethylanilineHCID 21904356—
용매DimethylformamideHCID 6228—
생성물[2-(benzyloxy)-5-(5H-pyrrolo[3,2-d]pyrimidin-4-ylamino)phenyl]methanolHCID 5759732140.3%

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온도80 °C

반응 단계

A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (307 mg), [5-amino-2-(benzyloxy)phenyl]methanol (459 mg) and N,N-dimethylformamide (10 mL) was stirred at 80° C. for 4 hrs. The reaction mixture was concentrated under reduced pressure, aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with ethyl acetate containing tetrahydrofuran. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent, methanol:ethyl acetate=0:100→30:70). Ethanol and ethyl acetate were added and the precipitate was collected by filtration to give the title compound (279 mg) as a brown powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08178543B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-b66d091d05e5401fb2b9115ccc1c792b
출처 메모uspto-grants-2012_05