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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20726생성일: 2026년 10월 25일

Water → 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamino)-methyl]-benzamide

https://huagongshe.com/reaction/20726

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물3,4-difluoro-2-(2-fluoro-4-iodoanilino)-N-(2-hydroxyethoxy)-5-[(E)-2-hydroxyethoxyiminomethyl]benzamideHCID 11307224—
용매MethanolHCID 887—
생성물3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamino)-methyl]-benzamideHCID 11577457—

반응 단계

To a solution of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyimino)-methyl]-benzamide (3.62 g, 6.70 mmol) obtained in Step B in methanol (100 ml) were added portionwise trifluoroacetic acid (6.5 ml) and sodium cyanoborohydride (3.78 g, 60.2 mmol) over 2 days while monitoring the progression of the reaction by TLC. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (CH2Cl2/MeOH (15:1)), and the resultant crude compound was crystallized from methylene chloride to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamino)-methyl]-benzamide (1.66 g, 46%, as a total of first and second crystals).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745663B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7d9fb428ff414262adbf4997cde31aae
출처 메모uspto-grants-2010_06