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HRID 249056생성일: 2026년 10월 25일

p-Toluenesulfonic acid → 2',3'-Didehydro-2',3'-dideoxyuridine

https://huagongshe.com/reaction/249056

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Sodium HydroxideHCID 14798—
반응물5'O-trityl-2',3'-dideoxy-2',3'-didehydrouridineHCID 11091653—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물2',3'-Didehydro-2',3'-dideoxyuridineHCID 65159—

반응 단계

5'O-trityl-2',3'-dideoxy-2',3'-didehydrouridine (0.5 gm.,1.1 mM) was dissolved in a chloroform (10 mL) and methanol (2 mL) mixture containing 2% p-toluenesulphonic acid. The reaction mixture was stirred at room temperature for 0.75 hr., and then neutralized with 2N NaOH (0.5 mL). The solvent was removed in vacuo and the residue chromatographed on silica using chloroform/acetone (2:1) as eluent. The desired product was isolated as a white crystalline solid with the same physical and spectroscopic characteristics as d4U produced by an alternative method. M.p. 155° C. 1H NMR (360 Mhz, D2O/DMSO) 7.8 (d, 1H, H6), 6.7 (m, 1H, H1'), 6.37 (m, 1H, H2'), 5.8 (m, 1H, H3'), 5.56 (d, 1H, H5), 4.7 (m, 1H, H4'), 3.6 (m, 2H, H5'). 13C NMR (70 Mhz, D2O/DMSO) 163 (C4), 151 (C2), 141 (C2'), 135 (C3'), 126 (C6), 101 (C5), 89 (C1'), 87 (C4'), 62 (C5').

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05212294
출처 데이터셋uspto-grants-1993_05
ORD IDord-7594f2a196c44593b7c5773cc7805d8c
출처 메모uspto-grants-1993_05