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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71211생성일: 2026년 10월 23일

Potassium Carbonate → Ethyl 2-amino-7-[3-methoxy-4-(2-methyl-1,3-oxazol-5-yl)phenyl]hept-6-ynoate

https://huagongshe.com/ko/reaction/71211

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 2-(diphenylmethyleneamino)acetateHCID 319508—
반응물5-[4-(5-Chloropent-1-yn-1-yl)-2-methoxyphenyl]-2-methyl-1,3-oxazoleHCID 66608267—
촉매Tetrabutylammonium IodideHCID 67553—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-amino-7-[3-methoxy-4-(2-methyl-1,3-oxazol-5-yl)phenyl]hept-6-ynoateHCID 6660870158.9%

반응 조건

온도80 °C

반응 단계

A mixture of 5-[4-(5-chloropent-1-yn-1-yl)-2-methoxyphenyl]-2-methyl-1,3-oxazole (500 mg), ethyl N-(diphenylmethylene)glycinate (461 mg), potassium carbonate (1.2 g) and tetrabutylammonium iodide (637 mg) in acetonitrile (5 mL) was stirred at 80° C. overnight under an argon atmosphere. The reaction mixture was diluted with ethyl acetate, the mixture was washed with water and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the residue, the insoluble material was separated by filtration, and the filtrate was concentrated. A mixture of the residue and 6N hydrochloric acid (0.5 mL) in acetonitrile (5 mL) was stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (362 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822699B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3bfd861b87a34d849b274b52e001c5a5
출처 메모uspto-grants-2014_09