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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2089629생성일: 2026년 10월 27일

Potassium Bicarbonate → Carbonic acid 1-(5-{(4-{amino[benzoylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxy)ethyl ester cyclohexyl ester

https://huagongshe.com/reaction/2089629

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참여 물질

역할이름HCID투입량
반응물Potassium BicarbonateHCID 516893—
반응물1-Chloroethyl Cyclohexyl CarbonateHCID 11229529—
반응물N-[1-amino-1-(4-{[[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl]amino}phenyl)methylidene]benzamideHCID 136334022—
용매DimethylformamideHCID 6228—
생성물Carbonic acid 1-(5-{(4-{amino[benzoylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxy)ethyl ester cyclohexyl esterHCID 6747116852.9%

반응 조건

온도55 °C

반응 단계

To a mixture of N-[1-amino-1-(4-{[[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl]amino}phenyl)methylidene]benzamide (Example 1a, 1.0 g) and DMF (20 mL), potassium hydrogen carbonate (1.67 g) and 1-chloroethyl cyclohexyl carbonate (2.76 g) were added, and the resulting mixture was stirred at 55° C. for 26 hours. The reaction solution was filtered, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate) to obtain the captioned compound (680 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08436009B2
출처 데이터셋uspto-grants-2013_05
ORD IDord-2b6ad9cf33da400599b25bbc2a97d622
출처 메모uspto-grants-2013_05