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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 5370695 | — |
| 반응물 | 4-Benzyloxy-3-hydroxymethylaniline | HCID 21904356 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [2-(benzyloxy)-5-(5H-pyrrolo[3,2-d]pyrimidin-4-ylamino)phenyl]methanol | HCID 57597321 | 40.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07507740B2 |
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| 출처 데이터셋 | uspto-grants-2009_03 |
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| ORD ID | ord-fad64d0f1a4e45a4b69194a647c21ad6 |
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| 출처 메모 | uspto-grants-2009_03 |
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