戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1085693作成日:2026年10月26日

4-Vinylpyridine → N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamine

https://huagongshe.com/reaction/1085693

反応式

関与物質

役割名称HCID仕込み量
反応物4-VinylpyridineHCID 7502—
反応物N-(4-piperidinyl)-2-benzoxazolamineHCID 14575294—
溶媒1-ButanolHCID 263—
生成物N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamineHCID 1457587062%

反応手順

A mixture of 3.2 parts of 4-(1-ethenyl)pyridine, 2.1 parts of N-(4-piperidinyl)-2-benzoxazolamine and 80 parts of 1-butanol was stirred and refluxed for 48 hours. The reaction mixture was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) saturated with ammonia, as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane, yielding 2 parts (62%) of N-[1-[2-(4-pyridinyl)ethyl]-4-piperidinyl]-2-benzoxazolamine; mp. 146.9° C. (450).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05010198
出典データセットuspto-grants-1991_04
ORD IDord-6f9201b8286849fbbca0c9ac6be90757
出典メモuspto-grants-1991_04