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HRID 727015作成日:2026年10月25日

1,2,3,5-Tetraacetyl-beta-D-ribofuranose → 2-Amino-5,6-dichloro-1-(2,3,5-tri-O-acetyl-beta-D-ribofuranosyl)benzimidazole

https://huagongshe.com/reaction/727015

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,5-Tetraacetyl-beta-D-ribofuranoseHCID 83064—
反応物2-Amino-5,6-dichlorobenzimidazoleHCID 466016—
反応物Trifluoromethyl(trimethylsilyl) sulfoneHCID 13257444—
溶媒AcetonitrileHCID 6342—
生成物2-Amino-5,6-dichloro-1-(2,3,5-tri-O-acetyl-beta-D-ribofuranosyl)benzimidazoleHCID 1004987615.5%

反応条件

温度60 °C

反応手順

2-Amino-5,6-dichlorobenzimidazole (4) (3 g, 16 mmole) was dissolved in dry acetonitrile (150 ml) and stirred in an inert atmosphere at 60° C. BSA (4.37 ml, 17 mmole) was added and the mixture was stirred for 10 minutes. 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose (5.09 g, 16 mmole) and TMSTf (3.29 ml, 17 mmole) were added to the clear solution and the mixture was allowed to stir at 60° C. for 1 hr. The mixture was concentrated under reduced pressure and separated on a silica column to yield 1.14 g (15%) of 2-amino-5,6-dichloro-1-(2,3,5,tri-O-acetyl-β-D-ribofuranosyl) benzimidazole (43). 13C NMR (CDCl3): d 170.04 ppm, 169.56, 169.11, 154.57, 141.64, 132.53, 125.90, 1123.45, 117.72, 109.49, 85.78, 80.99, 70.95, 69.83, 62.91, 20.74, 20.54, 20.20. 1H NMR (CDCl3): d 0.96 ppm (s, 3H), 1.09 (s, 3H), 1.13 (s, 3H), 3.75 (m, 2H), 4.08 (dd, 1H), 5.00 (dd, 1H), 5.13 (t, 1H), 5.42 (s, 2H), 5.61 (d, 1H), 7.27 (s, 1H), 7.42 (s, 1H). MS (FAB) m/e 758,718, 676, 460, 426, 259, 217, 139.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05712255
出典データセットuspto-grants-1998_01
ORD IDord-14c6da77682c4dbd9ad22c6c59fa8c6e
出典メモuspto-grants-1998_01