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HRID 249056作成日:2026年10月26日

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

https://huagongshe.com/reaction/249056

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Sodium HydroxideHCID 14798—
反応物5'O-trityl-2',3'-dideoxy-2',3'-didehydrouridineHCID 11091653—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
生成物2',3'-Didehydro-2',3'-dideoxyuridineHCID 65159—

反応手順

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').

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212294
出典データセットuspto-grants-1993_05
ORD IDord-7594f2a196c44593b7c5773cc7805d8c
出典メモuspto-grants-1993_05