戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1415151作成日:2026年10月25日

Phenyl(pyridin-3-yl)acetonitrile → 2-Phenyl-(3-pyridyl)-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrile

https://huagongshe.com/reaction/1415151

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl(pyridin-3-yl)acetonitrileHCID 270956—
反応物2-(2-Chloroethyl)-2-azabicyclo[2.2.2]octaneHCID 12612325—
溶媒TolueneHCID 1140—
生成物2-Phenyl-(3-pyridyl)-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrileHCID 20356966—

反応手順

α-Phenyl-3-pyridylacetonitrile (U.S. Pat. No. 3,225,054) is reacted with 2-(2-chloroethyl)-2-azabicyclo[2.2.2]octane in toluene to provide 2-phenyl-2-(3-pyridyl)-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrile. This nitrile is reacted with sodium azide in DMF containing lithium chloride to provide 5-[1-phenyl-1-(3-pyridyl)-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-1H-tetrazole. Reaction this tetrazole with acetic anhydride in pyridine provides 5-[1-phenyl-1-(3-pyridyl)-3-(2-azabicyclo[2.2.2]oct-2-yl)propyl]-2-methyl-1,3,4-oxadiazole, the oxalate salt melts at 171°-172° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04003904
出典データセットuspto-grants-1977_01
ORD IDord-0d9de3fef5174e15a1c0482c643ed40e
出典メモuspto-grants-1977_01