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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1295561생성일: 2026년 10월 25일

Triphenylphosphine → tert-Butyl 4-(2-oxo-1,2,3,4-tetrahydroquinolin-7-yloxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1295561

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Tert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
반응물7-Hydroxy-3,4-dihydrocarbostyrilHCID 2785758—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 4-(2-oxo-1,2,3,4-tetrahydroquinolin-7-yloxy)piperidine-1-carboxylateHCID 5757591029%

반응 단계

Triphenylphosphine (0.577 g, 2.2 mmol) was dissolved in dry tetrahydrofuran (20 mL) under argon and the solution cooled to 0–5° C. Diisopropyl azodicarboxylate (0.404 g, 2 mmol) was added dropwise and the mixture stirred at 0–5° C. for 20 min. before addition of 7-hydroxy-3,4-dihydro-1H-quinolin-2-one (0.326 g, 2 mmol) and 4-hydroxypiperidine-1-carboxylic acid tert-butyl ester (0.402 g, 2 mmol). The resulting mixture was stirred at ambient temperature for 18 h then evaporated to dryness under reduced pressure. Chromatography on SiO2, eluting with a gradient of ethyl acetate in 60–80° C. petroleum ether, gave the title compound (0.2 g, 29%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07244726B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-9a923ae1eea44fb293a53fe57e4be0a3
출처 메모uspto-grants-2007_07