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HRID 263871作成日:2026年10月26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/263871

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-βribofuranosyl)benzimidazole (43).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646125
出典データセットuspto-grants-1997_07
ORD IDord-67322e2591fb4d8b827a18c24b8db0c9
出典メモuspto-grants-1997_07