戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 373895作成日:2026年10月27日

Phthaloyl chloride → 9-Benzyloxy-6-phthalimidopurine

https://huagongshe.com/reaction/373895

反応式

関与物質

役割名称HCID仕込み量
反応物Phthaloyl chlorideHCID 6955—
反応物TriethylamineHCID 8471—
反応物9-(Benzyloxy)-9H-purin-6-amineHCID 12354493—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TetrahydrofuranHCID 8028—
生成物9-Benzyloxy-6-phthalimidopurineHCID 1452396949%

反応手順

Phthaloyl dichloride (13.35 g; 92.2 mmol) was added to a cooled solution of 9-benzyloxyadenine (14.9 g, 61.5 mmol), 4-dimethylaminopyridine (1.5 g, 12.3 mmol) and triethylamine (25.7 ml, 184.4 mmol) in tetrahydrofuran (200 ml). After 1 hour at room temperature the solvent was removed under reduced pressure and the residue partitioned between chloroform (500 ml) and saturated potassium bicarbonate (300 ml). The organic phase was separated, washed with water (200 ml), brine (200 ml), dried (MgSO4) and evaporated to dryness. Column chromatography on silica gel eluting with chloroform-methanol (100:1) afforded the title compound (11.20 g, 49%). IR: υmax (KBr) 3070, 1800, 1740, 1730, 1605, 1585, 1450 and 1410 cm-1 ; 1H NMR δH [(CD3)2SO] 5.70(2H, s, CH2Ph), 7.55(5H, s, CH2Ph), 8.20(4H, s, Ar), 8.95(1H, s, H-2), 9.25(1H, s, H-8). Found: C, 64.71; H, 3.78; N, 18.85%; m/z 371.1025. C20H13N5O3 requires: C, 64.68; H, 3.54; N, 18.86%; m/e 371.1018.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05166198
出典データセットuspto-grants-1992_11
ORD IDord-07fa810156e54e2b9a434faa8cb68b83
出典メモuspto-grants-1992_11