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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14066생성일: 2026년 10월 24일

Oxazole → N-Methyl-5-oxazol-2-yl-N-propyl-isophthalamic acid

https://huagongshe.com/ko/reaction/14066

반응식

참여 물질

역할이름HCID투입량
반응물OxazoleHCID 9255—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Methyl 3-iodo-5-{[methyl(propyl)amino]carbonyl}benzoateHCID 21086185—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Methanol tetrahydrofuran waterHCID 21892291—
생성물N-Methyl-5-oxazol-2-yl-N-propyl-isophthalamic acidHCID 21085840—

반응 조건

온도0 °C

반응 단계

To a −70° C. stirred solution of oxazole (330 mg, 4.8 mmol) in tetrahydrofuran (4 mL) is added n-butyllithium (1.6 M in hexanes, 3.3 mL, 5.3 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 14.5 mL, 14.5 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-iodo-5-{[methyl(propyl)amino]carbonyl}benzoate (1.6 g, 4.5 mmol) in anhydrous tetrahydrofuran (3 mL) followed by palladium(0)tetrakis(triphenylphosphine) (221 mg, 0.19 mmol). The reaction mixture is heated at reflux for 2 h. The reaction mixture is cooled, diluted with ethyl acetate, washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 60% ethyl acetate/hexane) provides a solid. The solid is redissolved in 1:1:1 tetrahydrofuran/methanol/water (9 mL), and lithium hydroxide monohydrate (311 mg, 7.4 mmol) is added and stirred 2 h at room temperature. The reaction is diluted in chloroform and washed with 1N hydrochloric acid (aq), water, and brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to give the title compound. ESI MS m/z 287.3 [M−H]−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727997B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d945e176239c4c6c9e6013b66b49819e
출처 메모uspto-grants-2010_06