HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 86591800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59118234 | HCID 59118234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86591800 | HCID 86591800 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919371B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-db0152cc82aa42dba7668b5608062745 |
| Source note | uspto-grants-2005_07 |