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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1354186생성일: 2026년 10월 27일

Ethanol → ethyl 8-(3-aminophenyl)-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate

https://huagongshe.com/reaction/1354186

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물3-Aminophenylboronic acid hydrochlorideHCID 2763241—
반응물ethyl 8-chloro-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylateHCID 12071709—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물ethyl 8-(3-aminophenyl)-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylateHCID 996895348.4%

반응 단계

92.7 mg of ethyl 8-chloro-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate was suspended in 1 ml of toluene. 0.5 ml of ethanol, 0.5 ml of 2 M aqueous sodium carbonate solution, 50 mg of 3-aminophenylboronic acid hydrochloride and 10 mg of bis(triphenylphosphine) palladium (II) chloride were added to the obtained suspension, and they were heated under reflux in argon atmosphere for 3 hours. Ethyl acetate was added to the reaction mixture. The organic layer was taken, washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The resultant residue was purified by the silica gel column chromatography (eluent: chloroform/ethyl acetate=4/1) to obtain 50.6 mg of ethyl 8-(3-aminophenyl)-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07223773B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-9c94fe53bdf64d809ce518414720261c
출처 메모uspto-grants-2007_05