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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727015생성일: 2026년 10월 25일

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

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-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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712255
출처 데이터셋uspto-grants-1998_01
ORD IDord-14c6da77682c4dbd9ad22c6c59fa8c6e
출처 메모uspto-grants-1998_01