HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl iodide → HCID 56975984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 57248052 | HCID 57248052 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 56975984 | HCID 56975984 | 52.7% |
Reaction Steps
To an ice cooled solution of 1-[(2S,3R)-2-benzyloxy-5-(6-chloroindol-1-yl)-3-pentyl]imidazole-4-carboxamide (47.9 mg, 0.110 mmol) in chloroform (5 ml) was added trimethylsilyl iodide (42.6 mg, 0.213 mmol). After 3 minutes, the ice bath was removed, and then stirred at room temperature for 3 hours. The reaction was quenched by addition of methanol. This mixture was extracted with ethyl acetate, and the extracts were washed with brine, dried (sodium sulfate) and evaporated in vacuo. The residue was purified by silica gel (1.5 g) chromatography eluting with chloroform/methanol (50:1 to 10:1) to give 1-[(2S,3R)-5-(6-chloroindol-1-yl)-2-hydroxy-3-pentyl]imidazole-4-carboxamide (20.1 mg, 52.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596738B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-58a016a26078479a88a5175169dd0201 |
| Source note | uspto-grants-2003_07 |