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HRID 2221095作成日:2026年10月25日

Sodium hydride → (Z)-Methyl 2-(benzyloxycarbonylamino)-3-(5-(tert-butoxycarbonyl amino)-2-phenylpyridin-4-yl)acrylate

https://huagongshe.com/reaction/2221095

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物Methyl 2-(((benzyloxy)carbonyl)amino)-2-(diethyl phosphono)acetateHCID 11068333—
反応物HCID 58671548HCID 58671548—
溶媒TetrahydrofuranHCID 8028—
生成物(Z)-Methyl 2-(benzyloxycarbonylamino)-3-(5-(tert-butoxycarbonyl amino)-2-phenylpyridin-4-yl)acrylateHCID 5867155042%

反応条件

温度0 °C

反応手順

To a slurry of 60% of sodium hydride (228 mg, 5.7 mmol) in THF (17 mL) at 0° C. was added 1A (1.88 g, 5.24 mmol) in several portions over 10 min. The reaction mixture was then brought to RT for 20 min, then cooled again at 0° C. A suspension of 3C (1.42 g, 4.76 mmol) in THF (17 mL) was added over 10 min at 0C, then the reaction was warmed up to RT. After stirring for 20 min, the reaction was quenched with water (40 mL). The aqueous layer was extracted with EtOAc (50 mL×2). The combined EtOAc extracts were dried (Na2SO4), filtered and concentrated. The resulting residue was purified by silica gel (110 g) column chromatography eluting with a gradient of EtOAc (0-60%) in hexane to give the title compound as an off-white solid (1 g, 42%). LC/MS (method A): retention time=3.33 min, (M+H)+=504.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07368458B2
出典データセットuspto-grants-2008_05
ORD IDord-cb1e9c6501204994b1b53696e03a67be
出典メモuspto-grants-2008_05