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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6251생성일: 2026년 10월 23일

Phthaloyl chloride → 9-Benzyloxy-6-phthalimidopurine

https://huagongshe.com/ko/reaction/6251

반응식

참여 물질

역할이름HCID투입량
반응물Phthaloyl chlorideHCID 6955—
반응물TriethylamineHCID 8471—
반응물9-(Benzyloxy)-9H-purin-6-amineHCID 12354493—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매TetrahydrofuranHCID 8028—
생성물9-Benzyloxy-6-phthalimidopurineHCID 1452396949%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247085
출처 데이터셋uspto-grants-1993_09
ORD IDord-9d6d039efa9945a3beb94d8cc151e292
출처 메모uspto-grants-1993_09