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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393601생성일: 2026년 10월 24일

Sodium Bicarbonate → HCID 22646584, 화합물

https://huagongshe.com/ko/reaction/393601

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물5-Benzyloxy-2-fluoro-4-methylphenolHCID 21991049—
반응물HCID 22646522HCID 22646522—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물HCID 22646584HCID 2264658463%

반응 조건

온도160 °C

반응 단계

4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline (187 mg, 0.71 mmol), (prepared as described for the starting material in Example 1 but with an aqueous sodium hydrogen carbonate work up), was added to a solution of 5-benzyloxy-2-fluoro-4-methylphenol (248 mg, 1 mmol), (prepared as described for the starting material in Example 3), and potassium t-butoxide (120 mg, 1 mmol) in DMSO (5 ml) and the mixture then heated at 160° C. for 1.5 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/ethyl acetate (55/45) followed by preparative reverse-phase HPLC eluting with aqueous ammonium carbonate (2 g/1, adjusted to pH7 with carbon dioxide) and methanol (20/80) to give 4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline (204 mg, 63%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809097B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-694d6787e78e4946aa91d24d25588844
출처 메모uspto-grants-2004_10