돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329405생성일: 2026년 10월 24일

Sodium Iodide → 4-(4-(4-(4-(3-Trifluoromethylphenyl)piperazinyl)butyl)-phenyl)-2-aminothiazole

https://huagongshe.com/ko/reaction/329405

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium CarbonateHCID 10340—
반응물DiisopropylethylamineHCID 81531—
반응물TFMPP hydrochlorideHCID 3084246—
반응물4-(4-(4-Chlorobutyl)phenyl)-2-aminothiazole hydrobromideHCID 14211429—
용매Methyl Isobutyl KetoneHCID 7909—
생성물4-(4-(4-(4-(3-Trifluoromethylphenyl)piperazinyl)butyl)-phenyl)-2-aminothiazoleHCID 14211430—

반응 단계

To a 125 ml round-bottomed flask equipped with condenser and N2 inlet were added 2.61 g (7.5 mmol) of 4-(4-(4-chlorobutyl)phenyl)-2-aminothiazole hydrobromide, 2.0 g (7.5 mmol) of N-(3-trifluoromethylphenyl)piperazine hydrochloride, 2.62 ml (15.0 mmol) of diisopropylethylamine, 1.59 g (15.0 mmol) of sodium carbonate, 5 mg of sodium iodide, and 50 ml of methylisobutylketone. The reaction was heated at reflux for 3.5 days, cooled, and the precipitate filtered, and the filtrate evaporated. The residue was chromatographed on silica gel using methylene chloride/ethyl acetate and ethyl acetate as eluents. The product fractions were concentrated, taken up in methylene chloride/methanol, precipitated by addition of ethyl acetate saturated with hydrochloride, evaporated, and the residue triturated with ether/ethyl acetate to afford a white solid, m.p. 174°-179° C., 0.87 g (23%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04891375
출처 데이터셋uspto-grants-1990_01
ORD IDord-b0d66922660d400b8d55e72f93b0914f
출처 메모uspto-grants-1990_01