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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14298생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/14298

반응식

참여 물질

역할이름HCID투입량
반응물OxazoleHCID 9255—
반응물Methyl 3-{[butyl(methyl)amino]carbonyl)-5-iodobenzoateHCID 21086165—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Methyl 3-{[butyl(methyl)amino]carbonyl}-5-(1,3-oxazol-2-yl)benzoateHCID 21086164—

반응 조건

온도0 °C

반응 단계

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]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f3b88abfac8942b69e60e949fb4b0ad9
출처 메모uspto-grants-2010_06