돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263871생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,5-Tetraacetyl-beta-D-ribofuranoseHCID 83064—
반응물2-Amino-5,6-dichlorobenzimidazoleHCID 466016—
반응물Trifluoromethyl(trimethylsilyl) sulfoneHCID 13257444—
용매AcetonitrileHCID 6342—
생성물2-Amino-5,6-dichloro-1-(2,3,5-tri-O-acetyl-beta-D-ribofuranosyl)benzimidazoleHCID 1004987615.5%

반응 조건

온도60 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646125
출처 데이터셋uspto-grants-1997_07
ORD IDord-67322e2591fb4d8b827a18c24b8db0c9
출처 메모uspto-grants-1997_07