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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13016생성일: 2026년 10월 24일

Triethylamine → N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(4-methylsulfanylphenyl)propan-2-yl]-2-methoxy-acetamide

https://huagongshe.com/ko/reaction/13016

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methoxyacetyl chlorideHCID 96623—
반응물(1R,2S)-1-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-[4-(methylthio)phenyl]propan-2-amine hydrochlorideHCID 66687724—
용매TetrahydrofuranHCID 8028—
생성물N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(4-methylsulfanylphenyl)propan-2-yl]-2-methoxy-acetamideHCID 25013491—

반응 단계

Methoxyacetyl chloride (10 μL, 0.11 mmol) was added to a suspension of (1R,2S)-1-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-[4-(methylthio)phenyl]propan-2-amine hydrochloride (40 mg, 0.09 mmol) and triethylamine (42 μL, 0.3 mmol) in THF (1 mL). The reaction was stirred at r.t. for 30 min and then quenched by adding water, the mixture was diluted with a small volume of MeCN so that a solution was obtained. This crude mixture was purified by semi-preparative HPLC using a Kromasil® C18 250×20 mm, 5 μm column. Flow 10 mL/min, 20 min gradient of 20%-90% MeCN in water followed by isocratic final concentration until product had eluted. UV=254 nm was used for detection. Fractions with product was combined and lyophilized to afford the title compound as a colourless solid. Yield 30 mg (69%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728030B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e5c732e75a6f47b9bb790ed140987727
출처 메모uspto-grants-2010_06