戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1708098作成日:2026年10月26日

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

https://huagongshe.com/reaction/1708098

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物diethyl (Z)-4-hydroxybut-1-enylphosphonateHCID 10081772—
反応物9-Hydroxy-6-phthalimidopurineHCID 14523970—
溶媒TetrahydrofuranHCID 8028—
生成物(Z)-9-[4-(diethoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurineHCID 1175451260%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05356886
出典データセットuspto-grants-1994_10
ORD IDord-2f7678df38634b6ab8fcf1b788e1e8a0
出典メモuspto-grants-1994_10