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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1512113생성일: 2026년 10월 24일

Triphenylphosphine → 3-Nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline

https://huagongshe.com/ko/reaction/1512113

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-PyrrolidineethanolHCID 76288—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물3-Nitroquinolin-6-olHCID 59507580—
용매TetrahydrofuranHCID 8028—
생성물3-Nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinolineHCID 5950759960%

반응 단계

6-Hydroxy-3-nitroquinoline (148 mg, 0.78 mmol) was dissolved in THF (18 mL). 2-(Pyrrolidin-1-yl)ethanol (0.091 mL, 0.78 mmol) and triphenylphosphine (306 mg, 1.17 mmol) were added. Lastly, diethyl azodicarboxylate (0.184 mL, 1.17 mmol) was added and the reaction mixture was allowed to stir at room temperature for 2 hours. The solvent was then concentrated in vacuo and the residue was purified by flash chromatography (SiO2) to yield 134 mg (60%) of 3-nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline. LC/MS (m/z): 288.1 (MH+), Rt 1.80 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217035B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-5f1d320b05c54b64b95ff23789ad63df
출처 메모uspto-grants-2012_07