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HRID 1856560作成日:2026年10月27日

Potassium Iodide → Astemizole

https://huagongshe.com/reaction/1856560

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium CarbonateHCID 10340—
反応物2-(4-Methoxyphenyl)ethyl methanesulfonateHCID 277977—
反応物Norastemizole hydrobromideHCID 3018631—
溶媒DimethylformamideHCID 6228—
生成物AstemizoleHCID 224748%

反応条件

温度70 °C

反応手順

A mixture of 2.3 parts of 2-(4-methoxyphenyl)ethyl methanesulfonate, 4.9 parts of 1-[(4-fluorophenyl)methyl]-N-(4-piperidinyl)-1H-benzimidazol-2-amine dihydrobromide, 3.2 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide is stirred overnight at 70° C. The reaction mixture is poured onto water. The product is extracted with methylbenzene. The extract is washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 2,2'-oxybispropane, yielding 2.2 parts (48%) of 1-(4-fluorophenylmethyl)-N-{1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl}-1H-benzimidazol-2-amine; mp. 172.9° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04219559
出典データセットuspto-grants-1980_08
ORD IDord-979daa0708dc452abb8295cefc7b72c8
出典メモuspto-grants-1980_08