돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1786923생성일: 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/1786923

반응식

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%

반응 조건

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 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 번호US07507740B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-fad64d0f1a4e45a4b69194a647c21ad6
출처 메모uspto-grants-2009_03