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HRID 6251作成日:2026年10月25日

Phthaloyl chloride → 9-Benzyloxy-6-phthalimidopurine

https://huagongshe.com/reaction/6251

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 chloroformmethanol (100:1) afforded the title compound (11.20 g, 49%). IR: νmax (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US05247085
出典データセットuspto-grants-1993_09
ORD IDord-9d6d039efa9945a3beb94d8cc151e292
出典メモuspto-grants-1993_09