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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 871994생성일: 2026년 10월 24일

1,4-Dioxane hydrochloride → 7-(4-Hydroxy-2-methoxyphenyl)-8-[N-(2-methoxyphenyl)-N-(9-fluorenylmethoxycarbonyl)aminomethyl]-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one

https://huagongshe.com/ko/reaction/871994

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참여 물질

역할이름HCID투입량
반응물1,4-Dioxane hydrochlorideHCID 20443148—
반응물7-(2-Methoxy-4-methoxymethoxyphenyl)-8-[N-(2-methoxyphenyl)-N-(9-fluorenylmethoxycarbonyl)aminomethyl]-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 58337196—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물7-(4-Hydroxy-2-methoxyphenyl)-8-[N-(2-methoxyphenyl)-N-(9-fluorenylmethoxycarbonyl)aminomethyl]-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-oneHCID 5833722156%

반응 단계

7-(2-Methoxy-4-methoxymethoxyphenyl)-8-[N-(2-methoxyphenyl)-N-(9-fluorenylmethoxycarbonyl)aminomethyl]-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one (Compound No. 12-1, 137 mg, 0.192 mmol) was dissolved in 1,4-dioxane (1 mL) and 4N hydrochloride/1,4-dioxane solution (144 μL, 0.576 mmol) was added thereto. After the reaction mixture was stirred at room temperature for 2 hours, the mixture was diluted with ethyl acetate (100 mL). The mixture was washed with water (100 mL) and saturated brine (50 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled compound (71.6 mg) as a colorless solid. (Yield 56%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975256B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-ba98da6075e24cd58b037269f671d355
출처 메모uspto-grants-2015_03