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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,2,3,5-Tetraacetyl-beta-D-ribofuranose | HCID 83064 | — |
| 反応物 | 2-Amino-5,6-dichlorobenzimidazole | HCID 466016 | — |
| 反応物 | Trifluoromethyl(trimethylsilyl) sulfone | HCID 13257444 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-Amino-5,6-dichloro-1-(2,3,5-tri-O-acetyl-beta-D-ribofuranosyl)benzimidazole | HCID 10049876 | 15.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05646125 |
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| 出典データセット | uspto-grants-1997_07 |
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| ORD ID | ord-67322e2591fb4d8b827a18c24b8db0c9 |
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| 出典メモ | uspto-grants-1997_07 |
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