戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1708092作成日:2026年10月25日

Triphenylphosphine → (E)-6-chloro-9-[4-(diisopropoxyphosphoryl)but-3-enyl]purine

https://huagongshe.com/reaction/1708092

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6-ChloropurineHCID 5359277—
反応物diisopropyl (E)-4-hydroxybut-1-enylphosphonateHCID 10399205—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-6-chloro-9-[4-(diisopropoxyphosphoryl)but-3-enyl]purineHCID 1006791437.2%

反応条件

温度0 °C

反応手順

To a mixture of 6-chloropurine (414 mg, 2.67 mmol), diisopropyl (E)-4-hydroxybut-1-enylphosphonate (630 mg, 2.67 mmol) and triphenyl phosphine (1.05 g, 4.00 mmol) in dry tetrahydrofuran (30 ml) stirred at 0° C. was added diethyl azodicarboxylate (0.70 g, 4.02 mmol). The mixture was allowed to warm to room temperature and stirred for 27.5 hr. The solvent was removed and the residue Was purified by column chromatography on silica gel eluting with dichloro-methane-methanol (24:1, 13:1) to give (E)-6-chloro-9-[4-(diisopropoxyphosphoryl)but-3-enyl]purine as a white solid (0.37 g, 37%), m.p. 105° C.; λmax (EtOH) 266 (9,260)nm; υmax (KBr) 3435, 2980, 1590, 1560, 1330, 1230 and 1210 cm-1 ; δH (CDCl3) 1.25 (12H, dd, J 6 Hz and 21 Hz, CH(CH3)2), 2.88 (2H, m, CH2), 4.45 (2H, t, J 7 Hz, CH2N), 4.55 (2H, m, CH(CH3)2), 5.68 (1H, dd, J 17 Hz and 20 Hz PCH=CH), 6.70 (1H, ddt, J 7 Hz, 17 Hz and 22 Hz, PCH=CH), 8.10 (1H, s, H-2/H-8), 8.77 (1H, s, H-2/H-8); FABMS (thioglycerol) 373 (MH+) (Found: C, 48.40; H, 6.03; N, 14.81%. C15H22ClN4O3P requires C, 48.33; H, 5.95; N, 15.03%).

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-2ce9467bafca43759eadb142f202b8f4
出典メモuspto-grants-1994_10