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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79481생성일: 2026년 10월 24일

Acetylcysteamine → 7-(2-acetamidoethylthio)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/ko/reaction/79481

반응식

참여 물질

역할이름HCID투입량
반응물AcetylcysteamineHCID 14484—
반응물Potassium tert-butoxideHCID 23665647—
반응물7-Fluoro-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamideHCID 67259826—
용매1,4-DioxaneHCID 31275—
생성물7-(2-acetamidoethylthio)-N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamideHCID 6833344058.3%

반응 조건

온도95 °C

반응 단계

N-(3-ethyl-1-((6-methylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-fluoroimidazo[1,2-a]pyridine-3-carboxamide (0.028 g, 0.065 mmol) (Example 74, Step A), N-(2-mercaptoethyl)acetamide (0.078 g, 0.65 mmol), and potassium tert-butoxide (0.022 g, 0.20 mmol) were added to a minimal amount of deoxygenated 1,4-dioxane in a sealed tube and heated for 18 hours at 95° C. The reaction mixture was cooled, concentrated under reduced pressure and purified by silica gel chromatography eluting with methanol (containing 6% ammonium hydroxide) and dichloromethane (1:9), to yield the product (20 mg) as a white powder. MS ESI (+) m/z 528 (M+1) detected.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841455B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-667f07dc02a9466c8e3966d61737eb20
출처 메모uspto-grants-2014_09