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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1022831생성일: 2026년 10월 25일

Triphenylphosphine → tert-butyl (6S,7S)-7-(4-chloro-3-fluorophenyl)-6-[(3-cyanopyridin-2-yl)oxy]-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022831

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물3-Cyano-2-pyridoneHCID 577543—
반응물tert-butyl (6R,7S)-7-(4-chloro-3-fluorophenyl)-6-hydroxy-1,4-oxazepane-4-carboxylateHCID 66976341—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl (6S,7S)-7-(4-chloro-3-fluorophenyl)-6-[(3-cyanopyridin-2-yl)oxy]-1,4-oxazepane-4-carboxylateHCID 6697665664.3%

반응 단계

Diisopropyl azodicarboxylate (1.9 M in toluene, 0.69 mL) was added dropwise to a solution of tert-butyl (6R,7S)-7-(4-chloro-3-fluorophenyl)-6-hydroxy-1,4-oxazepane-4-carboxylate (300 mg), triphenylphosphine (340 mg) and 2-oxo-1,2-dihydropyridine-3-carbonitrile (160 mg) in tetrahydrofuran (10 mL), and the mixture was stirred at room temperature for 4 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (250 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722662B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-ff26bb7785f54bb2bc00919d2c121f20
출처 메모uspto-grants-2014_05