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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1348794생성일: 2026년 10월 27일

Ammonium Chloride → 2-[2-(2-chlorophenyl)ethyl]-6-(4-fluoro-3-methylphenyl)-4-hydroxymethyl-2H-pyridazin-3-one

https://huagongshe.com/reaction/1348794

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참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Sodium borohydrideHCID 4311764—
반응물cerium(III) chloride hexahydrateHCID 22347666—
반응물2-[2-(2-chlorophenyl)ethyl]-6-(4-fluoro-3-methylphenyl)-4-methoxycarbonyl-2H-pyridazin-3-oneHCID 22562248—
용매MeOH tetrahydrofuranHCID 21899815—
생성물2-[2-(2-chlorophenyl)ethyl]-6-(4-fluoro-3-methylphenyl)-4-hydroxymethyl-2H-pyridazin-3-oneHCID 2256231911%

반응 단계

To a solution of 2-[2-(2-chlorophenyl)ethyl]-6-(4-fluoro-3-methylphenyl)-4-methoxycarbonyl-2H-pyridazin-3-one (480 mg, 1.20 mmol) in THF/methanol (2 mL/1 mL), cerium(III) chloride hexahydrate (425 mg, 1.20 mmol) was added at −15° C., followed by the addition of sodium borohydride (45 mg, 1.20 mmol). After stirred for 10 minutes, a saturated aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and was concentrated under reduced pressure. Further, the concentrate was purified by column chromatography on silica gel [hexane/ethyl acetate (2/1)] to yield the title compound as a pale yellow syrupy substance (yield: 11.0%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07211577B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-c90e3851495f4d1a8a68fb66a7e26226
출처 메모uspto-grants-2007_05