돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329394생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/329394

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물TriethylamineHCID 8471—
반응물Sodium CarbonateHCID 10340—
반응물TFMPP hydrochlorideHCID 3084246—
반응물4-(2-Chloroethyl)phenyl-2-aminothiazole hydrobromideHCID 14726983—
용매EthanolHCID 702—
생성물4-(4-(2-(4-(3-Trifluoromethylphenyl)piperazinyl)ethyl)phenyl)-2-aminothiazoleHCID 14211436—

반응 단계

To a 35 ml round-bottomed flask equipped with condenser and N2 inlet were added 0.81 g (2.55 mmol) of 4-(4-(2-chloroethyl)phenyl)-2-aminothiazole hydrobromide, 0.68 g (2.55 mmol) of N-(3-trifluoromethylphenyl)piperazine hydrochloride, 1.06 ml (7.64 mmol) of triethylamine, 0.27 g (2.55 mmol) of sodium carbonate, 2 mg of sodium iodide, and 10 ml of ethanol. The reaction was heated at reflux for 8 days, cooled, and the precipitate filtered, and the reaction mixture taken up in ethyl acetate/water. The layers were separated, the ethyl acetate washed with brine, dried, and evaporated to give a white solid, which was triturated with ethyl acetate. The solid was taken up in ethyl acetate/methanol, ether saturated with HCl added, the precipitate filtered, washed with ether, and dried to give a white solid, 0.255 g (18%), m.p. 274°-277° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04891375
출처 데이터셋uspto-grants-1990_01
ORD IDord-97602c7bc3e047e2802381429e7e193b
출처 메모uspto-grants-1990_01