Imidazole → HCID 86591800, compound

HRID 896867Notes

Reaction equation

HRID 896867 reaction equation
[OH:1][C@H:2]([C:24]1[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=1)[CH2:3][N:4]([CH2:12][C@H:13]1[CH2:22][CH2:21][C:20]2[C:15](=[CH:16][CH:17]=[C:18]([I:23])[CH:19]=2)[O:14]1)[C:5](=[O:11])[O:6][C:7]([CH3:10])([CH3:9])[CH3:8].[CH3:30][C:31]([Si:34](Cl)([CH3:36])[CH3:35])([CH3:33])[CH3:32].N1C=CN=C1.C([O-])(O)=O.[Na+]>CN(C=O)C>[Si:34]([O:1][C@H:2]([C:24]1[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=1)[CH2:3][N:4]([CH2:12][C@H:13]1[CH2:22][CH2:21][C:20]2[C:15](=[CH:16][CH:17]=[C:18]([I:23])[CH:19]=2)[O:14]1)[C:5](=[O:11])[O:6][C:7]([CH3:10])([CH3:8])[CH3:9])([C:31]([CH3:33])([CH3:32])[CH3:30])([CH3:36])[CH3:35]

Participants

6

Procedure

A mixture of tert-butyl (2R)-2-hydroxy-2-(3-pyridinyl)ethyl([(2R)-6-iodo-3,4-dihydro-2H-chromen-2-yl]methyl}carbamate (Example 37, Method A, 6.35 g, 12.4 mmol), TBDMSCl (2.25 g, 14.9 mmol) and imidazole (2.10 g, 30.9 mmol) in DMF (10 mL) was stirred at room temperature under argon for 24 hours. The reaction mixture was then poured into a saturated NaHCO3 solution (50 mL). The mixture was extracted with ether (100 mL×2). The ether layer was washed with water (50 mL) and dried over anhydrous sodium sulfate. Removal of the solvent in vacuo afforded a near white syrup which was purified by column chromatography (silica gel, hexanes/ethyl acetate (5/1, v/v)) giving the desired compound as a colorless oil. LC-MS m/z 625.0 (MH+), RT=4.09 minutes.

Workup

  1. extractionThe mixture was extracted with ether (100 mL×2)
  2. washThe ether layer was washed with water (50 mL)
  3. dry with materialdried over anhydrous sodium sulfate
  4. customRemoval of the solvent in vacuo
  5. customafforded a near white syrup which
  6. customwas purified by column chromatography (silica gel, hexanes/ethyl acetate (5/1

Sources & evidence

ORD record
ord-db0152cc82aa42dba7668b5608062745
Source dataset
uspto-grants-2005_07
Patent number
US06919371B2

Reaction notes

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