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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2263166생성일: 2026년 10월 25일

Water → N-imidazo[1,2-b]pyridazin-6-yl-4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide

https://huagongshe.com/reaction/2263166

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DiisopropylethylamineHCID 81531—
반응물1-(4-Phenyl-1,3-thiazol-2-yl)piperazineHCID 712468—
반응물2,2,2-Trichloroethyl imidazo[1,2-b]pyridazin-6-ylcarbamateHCID 68777877—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물N-imidazo[1,2-b]pyridazin-6-yl-4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamideHCID 6877808066.5%

반응 조건

온도70 °C

반응 단계

A mixture of 2,2,2-trichloroethyl imidazo[1,2-b]pyridazin-6-ylcarbamate (198 mg, 0.408 mmol), 1-(4-phenyl-1,3-thiazol-2-yl)piperazine (200 mg, 0.815 mmol) and diisopropylethylamine (0.076 ml, 0.408 mmol) in dimethylsulfoxide (2.7 ml) was stirred at 70° C. for 15 hours. Water was poured into the reaction solution, and the mixture was exacted 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 recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 110 mg (66.5%) 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-18d5184949fa4b83b40c7825b7ab8da9
출처 메모uspto-grants-2010_12