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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598715생성일: 2026년 10월 26일

Potassium Fluoride → [4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-oxo-acetic acid

https://huagongshe.com/reaction/598715

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물4-(5-Tri-butylstannanyl-pyridin-2-ylmethyl)-morpholineHCID 21136380—
반응물(4-Bromo-naphthalen-1-yl)-oxo-acetic acid methyl esterHCID 59379801—
촉매HCID 178418397HCID 178418397—
용매Ethyl AcetateHCID 8857—
용매1,3-DioxaneHCID 10450—
생성물[4-(6-Morpholin-4-ylmethyl-pyridin-3-yl)-naphthalen-1-yl]-oxo-acetic acidHCID 5937982354%

반응 조건

온도150 °C

반응 단계

4-(5-Tri-butylstannanyl-pyridin-2-ylmethyl)-morpholine (0.47 g, 1.59 mmol) and (4-Bromo-naphthalen-1-yl)-oxo-acetic acid methyl ester (18) (0.6 g, 1.3 mmol) and catalytic tetrakis(triphenylphosphine)palladium (0) were dissolved in 2 mL anhydrous 2,4-dioxane under nitrogen atmosphere. The tube was heated under microwave irradiation for 10 minutes at 150° C. After cooling to room temperature the mixture was diluted with EtOAc, and a solution of KF 40% was added. The organic phase was separated and the aqueous layer was evaporated and purified by LC-MS to afford the target product in 54% yield. Calculated mass=376. Observed mass=376.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897599B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-47264462ea5e422fbe2feac9d3fb334f
출처 메모uspto-grants-2011_03