HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 22878626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | HCID 54519329 | HCID 54519329 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22878626 | HCID 22878626 | — |
Reaction Steps
1′-Cyano-5′-(4,4′-dimethoxytrityl)thymidine in anhydrous pyridine is added to a stirred solution of t-butyldimethylchlorosilane (1.5 equivalents) and imidazole (3.0 equivalents) in anhydrous pyridine at 0° C. The resulting reaction mixture is stirred at room temperature overnight. Pyridine is evaporated and the residue dissolved in ethyl acetate, washed with brine. The crude is directly used for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06743902B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-ae53bcb2af1142f6a29a4bbd291a8c07 |
| Source note | uspto-grants-2004_06 |