Imidazole → HCID 66739120, compound

HRID 2213067Notes

Reaction equation

HRID 2213067 reaction equation
[OH:1][CH2:2][C@H:3]1[O:7][C:6](=[O:8])[CH2:5][CH2:4]1.N1C=CN=C1.[Si:14](Cl)([C:27]([CH3:30])([CH3:29])[CH3:28])([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>CN(C=O)C>[Si:14]([CH:2]([OH:1])[C@H:3]1[O:7][C:6](=[O:8])[CH2:5][CH2:4]1)([C:27]([CH3:30])([CH3:29])[CH3:28])([C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

5

Procedure

To a solution of 3 (7.0 g, 60 mmol) and imidazole (9.19 g, 135 mmol) in anhydrous DMF (70 mL) was added tert-butyldiphenylsilyl chloride (18.14 g, 66 mmol, 17.2 mL), and the solution was stirred at room temperature under a nitrogen atmosphere for 1 h. After removal of the solvent by evaporation, the residue was dissolved in CHCl3, washed with water and brine, dried (Na2SO4), filtered, and concentrated. After crystallization from hexane, the oily residue gave the title compound 4 as a white crystalline solid (20.6 g, 97%). M.P. 76° C.; 1H NMR (CDCl3) δ7.68–7.65 (m, 4H, arom.), 7.47–7.39 (m, 6H, arom.), 4.63–4.61 (m, 1H, H-5), 3.90–3.87 (dd, J=3 & 11 Hz, 1H, CH2OH), 3.70–3.67 (dd, J=3 & 11 Hz, 1H, CH2OH), 2.69–2.65 (m, 1H, H-3), 2.56–2.52 (m, 1H, H-3), 2.32–2.23 (m, 2H, H-4), 1.06 (s, 9H, t-Bu).

Workup

  1. customAfter removal of the solvent
  2. customby evaporation
  3. dissolutionthe residue was dissolved in CHCl3
  4. washwashed with water and brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customAfter crystallization from hexane

Sources & evidence

ORD record
ord-974edaaeace24eeb8e37a225d258f7c0
Source dataset
uspto-grants-2006_09
Patent number
US07105527B2

Reaction notes

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