Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1926012생성일: 2026년 10월 26일
N-methyl-2-pyrrolidone → N-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amine
https://huagongshe.com/reaction/1926012
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | 4-Benzyloxy-3-chloroaniline | HCID 1268285 | — |
| 반응물 | 4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 5370695 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | N-[4-(benzyloxy)-3-chlorophenyl]-5H-pyrrolo[3,2-d]pyrimidin-4-amine | HCID 57597271 | 49.5% |
반응 단계
A mixture of 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (200 mg), 4-(benzyloxy)-3-chloroaniline (365 mg) and 1-methyl-2-pyrrolidone (3 mL) was stirred at 80° C. for 4 hrs. Methanol and activated carbon were added to the reaction mixture and the mixture was stirred. The activated carbon was filtered off, aqueous sodium hydrogen carbonate solution was added and the mixture was extracted with ethyl acetate. The extract was washed with water and 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→15:75) and recrystallized from ethanol-ethyl acetate to give the title compound (226 mg) as a pale-brown powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08178543B2 |
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| 출처 데이터셋 | uspto-grants-2012_05 |
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| ORD ID | ord-c3bc6c71beef42a0b95fbac1f05738e5 |
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| 출처 메모 | uspto-grants-2012_05 |
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