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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15960생성일: 2026년 10월 24일

Lithium Hexamethyldisilazide → 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridazine-3-carboxamide

https://huagongshe.com/ko/reaction/15960

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물O-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
반응물Methyl 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 66673411—
용매TetrahydrofuranHCID 8028—
생성물4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridazine-3-carboxamideHCID 8660161599%

반응 단계

To a solution of methyl 4-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate (25 mg, 0.077 mmol) and O-(2-vinyloxy-ethyl)-hydroxylamine (24 mg, 0.23 mmol) in THF (2 mL) at 0° C. was added LiHMDS (0.54 mL, 0.54 mmol, 1 M in THF). The reaction mixture was warmed to room temperature and stirred for 1 hour. The reaction mixture was quenched with saturated aqueous NaHCO3 and diluted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude material that was purified by silica gel flash column chromatography (100% CH2Cl2 to 1.5% MeOH in CH2Cl2) to afford 30 mg (99%) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732616B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3b25464ef122462787f2fbae1dbb57ee
출처 메모uspto-grants-2010_06