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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2263173생성일: 2026년 10월 25일

Water → N-[6-(Acetylamino)pyridin-3-yl]-4-(5-methyl-4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide

https://huagongshe.com/reaction/2263173

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물5-Methyl-4-phenyl-2-piperazinyl-1,3-thiazoleHCID 17233868—
반응물2,2,2-Trichloroethyl[6-(acetylamino)pyridin-3-yl]carbamateHCID 86245259—
용매Dimethyl SulfoxideHCID 679—
생성물N-[6-(Acetylamino)pyridin-3-yl]-4-(5-methyl-4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamideHCID 6877944647.8%

반응 조건

온도70 °C

반응 단계

A mixture of 2,2,2-trichloroethyl [6-(acetylamino)pyridin-3-yl]carbamate (277 mg, 0.848 mmol), 1-(5-methyl-4-phenyl-1,3-thiazol-2-yl)piperazine (200 mg, 0.771 mmol) and diisopropylethylamine (0.148 ml, 0.848 mmol) in dimethylsulfoxide (2.6 ml) was stirred at 70° C. for 18 hours. 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 silica gel column chromatography (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 161 mg (47.8%) of the desired product as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07851473B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-37c81f786d24455b9f77d935f0c91186
출처 메모uspto-grants-2010_12