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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3650생성일: 2026년 10월 24일

Methanol → 5'-O-(4,4'-Dimethoxytrityl)thymidine

https://huagongshe.com/ko/reaction/3650

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물ThymidineHCID 5789—
반응물TriethylamineHCID 8471—
반응물1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
용매TetrahydrofuranHCID 8028—
생성물5'-O-(4,4'-Dimethoxytrityl)thymidineHCID 16241985.3%

반응 단계

Triethylamine (10 ml) in 200 ml THF was injected into a solid mixture of 6.8 g (28.0 mmol) thymidine and 10.2 g (28.6 mmol) 4,4'-dimethoxytrityl chloride under nitrogen with stirring. The solution was stirred at room temperature for 2 hours. After completion of the reaction, 10 ml methanol was added to consume the excess DMTrCl. The mixture was stirred for 5 minutes and the solvent removed by rotary evaporation. The residue was dissolved in 250 ml of ethyl acetate and the solution was washed with saturated NaHCO3 and dried over MgSO4. The solid was recrystallized from ethyl acetate/hexane to obtain 13.0 g 5'-protected thymidine 16 (85.6%).: m.p. 124°-126° C.; 1H NMR (200 MHz, CDCl3) δ8.97 (s, 1H, NH), 7.60 (m, 1H, H-6), 6.72-7.42 (m, 13H, Ph), 6.42 (m, 1H, H-1'), 4.56 (m, 1H, H-3'), 4.05 (m, 1H, H-4'), 3.78 (s, 6H, OMe2), 3.41 (m, 2H, H-5'), 2.62 (m, 1H, OH), 2.46 (m, 2H, H-2'), 1.46 (s, 3H, Me); 13C NMR (50 MHz, CDCl3) δ163.0 (C-4), 157.6, 149.8 (C-2), 143.5, 135.0 (C-6), 134.7, 134.6, 129.4, 127.4, 127.3, 126.5, 112.8, 110.9 (C-5), 86.7 (C-4'), 86.2, 84.7 (C-1'), 72.5 (C-3'), 63.8 (C-5'), 55.5 (OCH3), 41.3 (C-2'), 12.5 (CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734041
출처 데이터셋uspto-grants-1998_03
ORD IDord-2aa6ee52497c47eaaa4a3b64a6066424
출처 메모uspto-grants-1998_03