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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2263206생성일: 2026년 10월 26일

Water → 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]-N-pyridazin-3-ylpiperazine-1-carboxamide

https://huagongshe.com/reaction/2263206

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물1-[4-(4-Fluorophenyl)-2-thiazolyl]piperazineHCID 8027201—
반응물2,2,2-Trichloroethyl pyridazin-3-ylcarbamateHCID 68576698—
용매Dimethyl SulfoxideHCID 679—
생성물4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]-N-pyridazin-3-ylpiperazine-1-carboxamideHCID 6877845011.1%

반응 조건

온도70 °C

반응 단계

A mixture of 2,2,2-trichloroethyl pyridazin-3-ylcarbamate (226 mg, 0.835 mmol), 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]piperazine (200 mg, 0.760 mmol) and diisopropylethylamine (0.265 ml, 1.52 mmol) in dimethylsulfoxide (2.5 ml) was stirred at 70° C. for 3 days. Water was poured into the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by high performance liquid chromatography (YMC HPLC column; Solution A: 0.1% trifluoroacetic acid solution in acetonitrile; Solution B: 0.1% aqueous trifluoroacetic acid solution; eluted with 10% Solution A to 100% Solution A), and a saturated aqueous sodium hydrogen carbonate solution was added. The mixture was extracted with ethyl acetate. The extract was washed with water and dried over magnesium sulfate anhydrous, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and tetrahydrofuran to give the desired product (32.3 mg, 11.1%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07851473B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-303f3fef2cad4b8999fccc5fa6713003
출처 메모uspto-grants-2010_12