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Trimethylsilyl triflate → HCID 53700596、化合物

HRID 2227218
ノート
印刷プレビュー

反応式

HRID 2227218 の反応式
[Br:1][C:2]1[C:10]2[N:9]=[C:8]([Cl:11])[NH:7][C:6]=2[CH:5]=[C:4]([Cl:12])[C:3]=1[Cl:13].C/C(/O[Si](C)(C)C)=N\[Si](C)(C)C.C(O[CH:30]1[O:42][C@H:41]([CH3:43])[C@@H:36]([O:37][C:38](=[O:40])[CH3:39])[C@H:31]1[O:32][C:33](=[O:35])[CH3:34])(=O)C.C[Si](OS(C(F)(F)F)(=O)=O)(C)C>C(#N)C.C(OCC)(=O)C>[Br:1][C:2]1[C:10]2[N:9]=[C:8]([Cl:11])[N:7]([C@@H:30]3[O:42][C@H:41]([CH3:43])[C@@H:36]([O:37][C:38](=[O:40])[CH3:39])[C@H:31]3[O:32][C:33](=[O:35])[CH3:34])[C:6]=2[CH:5]=[C:4]([Cl:12])[C:3]=1[Cl:13]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 65367Trimethylsilyl triflateHCID 6913588N,O-bis(trimethylsilyl)acetamideHCID 11196237Tri-O-acetyl-5-deoxy-D-ribofuranoseHCID 18472159HCID 18472159、化合物

生成物 1

HCID 53700596HCID 53700596、化合物収率 55.9%

試薬・触媒・溶媒 2

HCID 6342
Acetonitrile
溶媒
2 回
HCID 8857Ethyl Acetate溶媒

反応条件

温度
65 °C

実験手順

To a suspension of 4-bromo-2,5,6-trichloro-1H-benzimidazole (0.30 g, 1 mmol), in acetonitrile (5 mL) was added N,O-bis(trimethylsilyl)acetamide (0.25 mL, 1 mmol). The resulting mixture was allowed to stir at 65° C. for 15 min., followed by the addition of 1,2,3-tri-O-acetyl-5-deoxyribofuranose (0.31 g, 1.2 mmol) in acetonitrile (5 mL) and trimethylsilyltrifluoromethane sulfonate (0.25 mL, 1.3 mmol). The mixture was allowed to stir at 65° C. for 20 min and was then allowed to cool to RT. The mixture was diluted with ethyl acetate and was washed with a saturated NaHCO3/NaCl solution, dried over MgSO4 and the solvents were removed by rotary evaporation. The product was purified by flash chromatography using chloroform as eluent followed by recrystallization from methanol to provide 0.28 g (55%) of the title compound as white crystals; m.p. 138-141° C.; 1H NMR (DMSO-d6) δ: 8.18 (s, 1H), 6.19 (d, 1H), 5.61 (dd, 1H), 5.25 (dd, 1H), 4.24 (m, 1H), 2.14 (s, 3H), 2.02 (s, 3H), 1.50 (d, 3H).

後処理

  1. stirringto stir at 65° C. for 20 min
  2. temperatureto cool to RT
  3. washwas washed with a saturated NaHCO3/NaCl solution
  4. dry with materialdried over MgSO4
  5. customthe solvents were removed by rotary evaporation
  6. customThe product was purified by flash chromatography
  7. customfollowed by recrystallization from methanol

出典と根拠

ORDレコード
ord-62129636baaf43248e9cfa8bf5b031cc
出典データセット
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06413938B1

反応ノート

読み込み中…

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