Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6251Generated: October 25, 2026

Phthaloyl chloride → 9-Benzyloxy-6-phthalimidopurine

https://huagongshe.com/reaction/6251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthaloyl chlorideHCID 6955—
ReactantTriethylamineHCID 8471—
Reactant9-(Benzyloxy)-9H-purin-6-amineHCID 12354493—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product9-Benzyloxy-6-phthalimidopurineHCID 1452396949%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05247085
Source datasetuspto-grants-1993_09
ORD IDord-9d6d039efa9945a3beb94d8cc151e292
Source noteuspto-grants-1993_09