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HRID 15982作成日:2026年10月26日

Lithium Hexamethyldisilazide → 5-fluoro-2-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridine-3-carboxamide

https://huagongshe.com/reaction/15982

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物O-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
反応物Methyl 5-fluoro-2-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydro-pyridine-3-carboxylateHCID 66673936—
溶媒TetrahydrofuranHCID 8028—
生成物5-fluoro-2-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-N-(2-(vinyloxy)ethoxy)-1,6-dihydropyridine-3-carboxamideHCID 86612534—

反応手順

To a mixture of methyl 5-fluoro-2-(2-fluoro-4-(methylthio)phenylamino)-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate (0.100 g, 0.294 mmol) and O-(2-(vinyloxy)ethyl)hydroxylamine (0.045 ml, 0.441 mmol) in THF (2 mL) at 0° C. was added lithium bis(trimethylsilyl)amide (1.18 ml, 1.18 mmol, 1 M solution in hexanes) dropwise. The reaction mixture was stirred for 20 minutes, quenched with 1 M HCl, and then partitioned between EtOAc and sat NaCl. The layers were separated and the aqueous layer was backextracted with EtOAc (1×). The combined organic layers were dried (Na2SO4), filtered and concentrated under reduced pressure to yield a crude yellow solid that was used without purification in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732616B2
出典データセットuspto-grants-2010_06
ORD IDord-b9b94b3733a74cc9974263223fb72f18
出典メモuspto-grants-2010_06