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HRID 1708098생성일: 2026년 10월 26일

Triphenylphosphine → (Z)-9-[4-(diethoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurine

https://huagongshe.com/reaction/1708098

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물diethyl (Z)-4-hydroxybut-1-enylphosphonateHCID 10081772—
반응물9-Hydroxy-6-phthalimidopurineHCID 14523970—
용매TetrahydrofuranHCID 8028—
생성물(Z)-9-[4-(diethoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurineHCID 1175451260%

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온도0 °C

반응 단계

To a mixture of 9-hydroxy-6-phthalimidopurine (320 mg, 1.14 mmol) , diethyl (Z)-4-hydroxybut-1-enylphosphonate (250 mg, 1.20 mmol) and triphenyl phosphine (448 mg, 1.71 mmol) in dry tetrahydrofuran (11 ml) stirred at 0° C. under dry nitrogen was added diethyl azodicarboxylate (296 mg, 170 mmol). The mixture was allowed to warm to r.t. and stirred for 2.3 hr. The solvent was removed and the residue was purified by column chromatography on silica gel eluting with acetone-hexane (1:1, 4:3) to give (Z)-9-[4-(diethoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurine as a light brown gum (320 mg, 60%); λmax (EtOH) 271 (14,680)nm; υmax (KBr) 2980, 1735, 1595, 1575, 1360, 1330, 1245 and 1025 cm-1 ; δH [(CD3)2SO] 1.23 (6H, t, J 7 Hz, CH3), 3.05 (2H, m, CH2), 3.98 (4H, dq, J 7 Hz and 8Hz, CH2CH 3), 4.63 (2H, t, J 6 Hz, CH2O ), 5.90 (1H, dd, J 14 Hz and 20 Hz, PCH=CH), 6.75 (1H, ddt, J 7 Hz, 14 Hz and 52 Hz, PCH=CH), 8.05 (4H, m, C6H4), 9.05 (1H, s, H-2/H-8), 9.10 (1H, s, H-2/H-8) (Found: C, 53.77; H, 4.87; N, 14.52%; MH+ 472.1384. C21H22N5O6P requires C, 53.50; H, 4.70; N, 14.86%; MH+ 472.1386).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05356886
출처 데이터셋uspto-grants-1994_10
ORD IDord-2f7678df38634b6ab8fcf1b788e1e8a0
출처 메모uspto-grants-1994_10