Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256664생성일: 2026년 10월 26일
1-Bromo-1-propene → 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine
https://huagongshe.com/reaction/256664
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-Bromo-1-propene | HCID 11533 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine | HCID 19785343 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine | HCID 19785242 | 22% |
반응 단계
A mixture of 1.2 parts of bromo-1-propene, 3.26 parts of 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine, 1.5 parts of sodium hydrogen carbonate and 40 parts of ethanol was stirred for 1 hour at reflux temperature. The reaction mixture was filtered over diatomaceous earth while hot and the filtrate was evaporated. The residue was taken up in water and the product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 0.8 parts (22%) of 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine; mp. 144.8° C. (compound 120).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05258380 |
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| 출처 데이터셋 | uspto-grants-1993_11 |
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| ORD ID | ord-6a068b16c7e5448499de677d54ff443f |
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| 출처 메모 | uspto-grants-1993_11 |
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