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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

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-1-propeneHCID 11533—
반응물Sodium BicarbonateHCID 516892—
반응물9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amineHCID 19785343—
용매EthanolHCID 702—
생성물9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amineHCID 1978524222%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258380
출처 데이터셋uspto-grants-1993_11
ORD IDord-6a068b16c7e5448499de677d54ff443f
출처 메모uspto-grants-1993_11