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HRID 14298作成日:2026年10月25日

Oxazole → Methyl 3-{[butyl(methyl)amino]carbonyl}-5-(1,3-oxazol-2-yl)benzoate

https://huagongshe.com/reaction/14298

反応式

関与物質

役割名称HCID仕込み量
反応物OxazoleHCID 9255—
反応物Methyl 3-{[butyl(methyl)amino]carbonyl)-5-iodobenzoateHCID 21086165—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 3-{[butyl(methyl)amino]carbonyl}-5-(1,3-oxazol-2-yl)benzoateHCID 21086164—

反応条件

温度0 °C

反応手順

To a −70° C. stirred solution of oxazole (167 mg, 2.4 mmol) in tetrahydrofuran (4 mL) is added n-butyllithium (1.6 M in hexanes, 1.7 mL, 2.7 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 7.3 mL, 7.3 mmol) is added and the reaction mixture is warmed to 0° C. for 1 h. To this mixture is added a solution of methyl 3-{[butyl(methyl)amino]carbonyl}-5-iodobenzoate (864 mg, 2.3 mmol) in anhydrous tetrahydrofuran (3 mL) followed by palladium(0)tetrakis(triphenylphosphine) (112 mg, 0.10 mmol). The reaction mixture is heated at reflux for 1.5 h. The reaction mixture is cooled, diluted with ethyl acetate, washed with water, and saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 60% ethyl acetate/hexane) provides the title compound. ESI MS m/z 317.1 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727997B2
出典データセットuspto-grants-2010_06
ORD IDord-f3b88abfac8942b69e60e949fb4b0ad9
出典メモuspto-grants-2010_06