돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1785382생성일: 2026년 10월 26일

Ethyl Acetate → 2-(4,6-Dimethoxypyrimidine-2-ylcarbonyl)aniline

https://huagongshe.com/reaction/1785382

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물OzoneHCID 24823—
반응물3-(4,6-Dimethoxypyrimidine-2-yl)-2-methylindoleHCID 12979368—
용매WaterHCID 962—
생성물2-(4,6-Dimethoxypyrimidine-2-ylcarbonyl)anilineHCID 1785675046%

반응 단계

In a reactor were placed 0.60 g (22 m moles) of 3-(4,6-dimethoxypyrimidine-2-yl)-2-methylindole and 20 ml of ethyl acetate. Thereinto was blown ozone at 0° C. to 10° C. for 4 hours. Thin-layer chromatography was conducted to confirm the disappearance of 3-(4,6-dimethoxypyrimidine-2-yl)-2-methylindole and complete a reaction. Then, the reaction mixture was heated to room temperature and concentrated. To the concentrate were added 20 ml of methanol and 5 ml of 6 N hydrochloric acid, and refluxing was made for 1 hour with heating. After the completion of the reaction, the reaction mixture was cooled to room temperature. 100 ml of water was added. The mixture was made alkaline with an aqueous sodium hydroxide solution, and extraction was made with ethyl acetate. The organic layer was concentrated. The concentrate was subjected to column chromatography separation to obtain 0.26 g (10 m moles) of 2-(4,6-dimethoxypyrimidine-2-ylcarbonyl)aniline. Yield: 46%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07504503B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-e56f0fa679da49f997b3678573607a0e
출처 메모uspto-grants-2009_03