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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 643010생성일: 2026년 10월 25일

N,N'-Dimethylethylenediamine → 5-Chloro-N-((1-(5-(2-oxopyridin-1(2H)-yl)pyridin-2-yl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/643010

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참여 물질

역할이름HCID투입량
반응물N,N'-DimethylethylenediamineHCID 8070—
반응물Potassium CarbonateHCID 11430—
반응물N-((1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methyl)-5-chlorothiophene-2-carboxamideHCID 68507465—
반응물HCID 178516071HCID 178516071—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
용매1,4-DioxaneHCID 31275—
생성물5-Chloro-N-((1-(5-(2-oxopyridin-1(2H)-yl)pyridin-2-yl)-1H-imidazol-4-yl)methyl)thiophene-2-carboxamideHCID 249872596.6%

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온도110 °C

반응 단계

A mixture of N-((1-(5-bromopyridin-2-yl)-1H-imidazol-4-yl)methyl)-5-chlorothiophene-2-carboxamide (42 mg, 0.11 mmol), 2-hydroxypyridine (40 mg, 0.42 mmol), N,N′-dimethylethylenediamine (0.035 mL, 0.32 mmol) and K2CO3 (52 mg, 0.38 mmol) in DMSO (1 mL) and dioxane (1 mL) was degassed with Argon before being charged with CuI (23 mg, 0.12 mmol). The mixture was heated at 110° C. overnight in a sealed tube. It was then purified by HPLC to give the title compound (3 mg). MS found for C19H14ClN5O2S: 412.2 and 414.2 (M+H, Cl pattern).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696352B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-3de329def22e45adb61ceacb273dc475
출처 메모uspto-grants-2010_04