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HRID 256667作成日:2026年10月26日

2-Vinylpyridine → 9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-pyridinyl)ethyl]-4-piperidinyl]-9H-purin-8-amine

https://huagongshe.com/reaction/256667

反応式

関与物質

役割名称HCID仕込み量
反応物2-VinylpyridineHCID 7521—
反応物9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amineHCID 19785343—
溶媒1-ButanolHCID 263—
生成物9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-pyridinyl)ethyl]-4-piperidinyl]-9H-purin-8-amineHCID 1978531615%

反応手順

A mixture of 1.93 parts of 2-ethenylpyridine, 5 parts of 9-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-9H-purin-8-amine and 80 parts of 1-butanol was stirred and refluxed overnight. The reaction mixture was evaporated. The residue was purified by column chromatography over silica gel using first a mixture of trichloromethane and methanol (95:5 by volume) and then 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, yielding 1 part (15%) of 9-[(4-fluorophenyl)methyl]-N-[1-[2-(2-pyridinyl)ethyl]-4-piperidinyl]-9H-purin-8-amine; mp. 172.3° C. (compound 141).

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-ccdd89b5515d4a498840c794f604ab87
出典メモuspto-grants-1993_11