돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483574생성일: 2026년 10월 25일

Pyridine → N-[4-(2-methyl-1H-imidazol-1-yl)phenyl]-4-(tetradecyloxy)benzeneacetamide

https://huagongshe.com/reaction/483574

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-(2-methyl-1H-imidazol-1-yl)anilineHCID 3157478—
반응물p-TetradecyloxyphenylacetylchlorideHCID 10021844—
용매TetrahydrofuranHCID 8028—
생성물N-[4-(2-methyl-1H-imidazol-1-yl)phenyl]-4-(tetradecyloxy)benzeneacetamideHCID 1503016258.3%

반응 단계

To a solution of 5.0 g of p-tetradecyloxy phenylacetyl chloride in 50 ml of tetrahydrofuran is added to a solution of 4.31 g of pyridine and 2.36 g of 4-(2-methyl-1H-imidazol-1-yl)benzenamine in 50 ml of tetrahydrofuran over 5 minutes. The mixture is stirred at ambient temperature for 1 hour, heated to reflux and allowed to stir at room temperature for 2 hours. The solvent is evaporated to a residue which is partitioned between chloroform and dilute sodium bicarbonate. The organic layer is separated, washed with water, dried and filtered through a pad of magnesium silicate. The solvent is evaporated to an oil which crystallizes from methyl alcohol:water to give 4.0 g of white solid Which is chromatographed on silica gel using ethyl acetate containing 0.1% ammonium hydroxide to give 3.9 g of the desired product as a white solid, m.p. 106°-109° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05225425
출처 데이터셋uspto-grants-1993_07
ORD IDord-ea21e8825c33429fa7ccfbd8f74d2288
출처 메모uspto-grants-1993_07