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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1856560생성일: 2026년 10월 26일

Potassium Iodide → Astemizole

https://huagongshe.com/reaction/1856560

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Sodium CarbonateHCID 10340—
반응물2-(4-Methoxyphenyl)ethyl methanesulfonateHCID 277977—
반응물Norastemizole hydrobromideHCID 3018631—
용매DimethylformamideHCID 6228—
생성물AstemizoleHCID 224748%

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04219559
출처 데이터셋uspto-grants-1980_08
ORD IDord-979daa0708dc452abb8295cefc7b72c8
출처 메모uspto-grants-1980_08