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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559585생성일: 2026년 10월 24일

8-Hydroxyquinoline → 5-chloro-N-((1-(4-(3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide

https://huagongshe.com/ko/reaction/559585

반응식

참여 물질

역할이름HCID투입량
반응물8-HydroxyquinolineHCID 1923—
반응물Potassium CarbonateHCID 11430—
반응물3-MethyluracilHCID 79066—
반응물5-Chloro-N-((1-(4-iodophenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamideHCID 24986897—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
생성물5-chloro-N-((1-(4-(3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)phenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamideHCID 2476016122.6%

반응 조건

온도130 °C

반응 단계

A mixture of 5-chloro-N-((1-(4-iodophenyl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide 1-6 (66 mg, 0.15 mmol), 3-methyluracil (60 mg, 0.48 mmol), 8-hydroxyquinoline (10 mg, 0.069 mmol) and K2CO3 (60 mg, 0.43 mmol) in DMSO (1 mL) was degassed with Ar before being charged with CuI (15 mg, 0.079 mmol). The mixture in a sealed tube was heated at 130° C. overnight. The mixture was then purified by HPLC to give the titled compound (15 mg). MS 442.2 and 444.2 (M+H, Cl pattern).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063077B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-f6632a6f1a684812871b6bebd0e33e71
출처 메모uspto-grants-2011_11