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HRID 256664作成日:2026年10月26日

1-Bromo-1-propene → 9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amine

https://huagongshe.com/reaction/256664

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-1-propeneHCID 11533—
反応物Sodium BicarbonateHCID 516892—
反応物9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amineHCID 19785343—
溶媒EthanolHCID 702—
生成物9-[(4-fluorophenyl)methyl]-N-[1-(2-propenyl)-4-piperidinyl)-9H-purin-8-amineHCID 1978524222%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258380
出典データセットuspto-grants-1993_11
ORD IDord-6a068b16c7e5448499de677d54ff443f
出典メモuspto-grants-1993_11