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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1708089생성일: 2026년 10월 25일

Triphenylphosphine → (E)-9-[4-(diisopropoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurine

https://huagongshe.com/reaction/1708089

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물diisopropyl (E)-4-hydroxybut-1-enylphosphonateHCID 10399205—
반응물9-Hydroxy-6-phthalimidopurineHCID 14523970—
용매TetrahydrofuranHCID 8028—
생성물(E)-9-[4-(diisopropoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurineHCID 1025538180.1%

반응 조건

온도0 °C

반응 단계

To a mixture of 9-hydroxy-6-phthalimidopurine (141 mg, 500 μmol), diisopropyl (E)-4-hydroxybut-1-enylphosphonate (110 g, 500 μmol) and triphenylphosphine (197 mg, 750 μmol) in tetrahydrofuran (5 ml) stirred at 0° C. was added diethyl azodicarboxylate (131 mg, 750 μmol). The mixture was then stirred at room temperature for 2 hr. The solvent was removed and the residue purified by column chromatography on silica gel eluting with dichloromethane-methanol (49:1, 16:1) to give (E)-9-[4-(diisopropoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurine as a gum (200 mg, 80%); λmax (EtOH) 273 (14,380) nm; υmax (film) 2970, 1730 1590 1570 1355 1240 and 975 cm-1 ; δH [(CD3)2SO] 1.24 (12H, pseudo t, J 6 Hz, CH(CH3)2), 2.77 (2H, m, CH2), 4 60 (2H, m, CH(CH3)2), 4.66 (2H, t, J 6 Hz, CH2O ), 6.07 (1H, dd, J 17 Hz and 20 Hz, PCH=CH), 6.75 (1H, ddt, J 6 Hz, 17 Hz and 22 Hz, PCH=CH), 8.00-8.25 (4H, m, Ph), 9.00 (1H, s, H-2/H-8), 9.08 (1H, s, H-2/H-8) (Found: M+ 499. 1620. C23H26N5O6P requires M+ 499.1621).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05356886
출처 데이터셋uspto-grants-1994_10
ORD IDord-c8fc4f318b8f4baeb437446062b6ae15
출처 메모uspto-grants-1994_10