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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52015생성일: 2026년 10월 23일

Dimedone → 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2yl)oxy]-2-methylindol-4-carboxylic Acid

https://huagongshe.com/ko/reaction/52015

반응식

참여 물질

역할이름HCID투입량
반응물DimedoneHCID 31358—
반응물Allyl 3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2-yl)oxy]-2-methylindol-4-carboxylateHCID 19962751—
용매TetrahydrofuranHCID 8028—
생성물3-Acetylamino-5-[(4,6-dimethoxypyrimidin-2yl)oxy]-2-methylindol-4-carboxylic AcidHCID 1996275493%

반응 단계

0.49 g of allyl 3-acetylamino-5-[(4,6-dimethoxypyrimidin-2-yl)oxy]-2-methylindol-4-carboxylate was dissolved in 10 ml of tetrahydrofuran, and 0.1 g of dimedone and 0.01 g of tetrakistriphenylphosphine palladium were added thereto. The mixture was stirred at room temperature for 4 hours. Crystals obtained by concentration under reduced pressure, was washed with isopropyl ether to obtain 0.41 g (yield: 93%) of the desired compound. mp: 230°-233° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616537
출처 데이터셋uspto-grants-1997_04
ORD IDord-d8978749e11948fcb45208fd1bc39b1f
출처 메모uspto-grants-1997_04